| GUAIFENESIN
TREATMENT & INFORMATION |
Guaifenesin
Treatment
by R. Paul St. Amand, M.D.
Over the
past 37 years, I have successfully treated 3,500 fibromyalgia patients
with several uricosuric (gout) drugs including, most recently, the simple
medication, guaifenesin. Many of my patients have also had vulvodynia,
which I consider part of the disease.
Symptoms
of Fibromyalgia
Among the many symptoms of fibromyalgia, the most prominent
are pain and stiffness in the muscles, tendons, and ligaments. Other
common symptoms include fatigue, irritability, depression, poor memory,
and lack of concentration. Fibromyalgics typically also suffer with
irritable bowel syndrome, urethral syndrome, painful intercourse, headaches
(often one-sided), burning hands and feet, and more. In short, people
with fibromyalgia have a lot of complaints.
Fibromyalgia appears to be an inherited biochemical abnormality that
primarily affects women. Symptoms can develop at any age, including
childhood, and progress in cycles. At first, they may be mild, with
long gaps or remissions between attacks. Eventually, however, the symptoms
worsen, with no more good days in between the bad days.
After patients begin taking guaifenesin, the symptoms reverse as they
developed, in cycles, but several times faster — like rewinding
a videotape of one's illness. Unfortunately, they often are worse than
before, since the reversal involves many areas simultaneously. Gradually
and progressively, however, more good days appear, cluster together,
and the patient is finally restored to normal. My experience is that
about two months at the proper dosage reverses at least one year of
accumulated disease.
Treatment
and Theory
Guaifenesin, a drug used to liquefy mucus, is mildly
uricosuric. Uricosuric drugs are used to treat gout by causing urinary
excretion of uric acid. Many years ago, quite by accident, I discovered
that uricosuric drugs also work for fibromyalgia. (I must stress, however,
that fibromyalgia and gout have no connection.) Unlike the potent uricosuric
drugs used in the past, guaifenesin has few, if any, side effects.
Having stumbled onto an effective treatment, it seemed appropriate to
formulate a theory based on the results. Upon analyzing twenty-four
hour urine collections in a few patients, before and after treatment,
I found a significant increase in the excretion of phosphate and a moderate
increase of oxalate and calcium after guaifenesin was started. I suspected
that the body cells of fibromyalgics retain abnormal amounts of substances
that should have been excreted by the kidneys. This abnormality, which
may be due to an inherited enzymatic deficiency, leads to symptoms fibromyalgics
experience in so many tissues and systems of the body.
My hypothesis, which is subject to further research, is that an excess
of intracellular phosphate, and possibly oxalate, builds up in cells
and depresses formation of energy (ATP) in the cells' "power stations,"
the mitochondria. Other researchers have discovered multiple biochemical
abnormalities in connection with fibromyalgia.
Management
Facts
The required dosage of guaifenesin is determined by patient
response. It varies from 300 mg. twice a day to as high as 3,600 mg
per day. Guaifenesin has been used for over twenty years; has no significant,
listed side effects; and is safe for children.
Treatment progress is measured both by symptom improvement and by filling
in body maps showing the location and size of tender points, spasms,
or hard patches felt in the muscles and ligaments. As guaifenesin "clears"
fibromyalgia out of the body, these patches decrease in size and eventually
disappear.
Aspirin & Aloe: A key aspect of treatment is that salicylates, contained
in aspirin and other compounds, completely block the effects of all
uricosuric drugs, including guaifenesin. Moreover, skin readily absorbs
salicylates into the body. Salicylates are manufactured by all plants,
the choicest parts of which are concentrated to make herbal medications,
many cosmetics, and deodorants.
Thus, patients being treated with guaifenesin cannot take aspirin or
herbal medications, or use any skin creams or topical products which
contain herbs, including aloe. Castor oil, Listerine, Ben Gay, and razors
with aloe strips are among the many culprits that block the action of
guaifenesin. When blocking occurs, patients have no adverse effects;
they simply obtain no benefit for fibromyalgia.
Hypoglycemia: Another complicating factor in guaifenesin treatment is
hypoglycemia, or "low blood sugar," better defined as carbohydrate
intolerance. Some of the many symptoms of hypoglycemia are tiredness,
panic, palpitations, and lightheadedness after eating sugar or starch.
Hypoglycemia can be controlled by a strict diet that eliminates sugar,
most carbohydrates, and caffeine.
As an endocrinologist, I see many hypoglycemics and have found that
around 40% of my fibromyalgia patients are hypoglycemic. It is mandatory
that the two syndromes be treated concurrently, or the patient will
not feel better. The added energy drain of hypoglycemia, untreated,
can also make guaifenesin treatment intolerable.
Maintenance Dosage: Since inherited abnormalities like fibromyalgia
cannot be cured, only controlled, patients must take guaifenesin for
the rest of their lives, or the symptoms will return. Therefore, a maintenance
dosage is necessary, usually the same amount it took to clear them.
Some of my earliest patients have been taking uricosuric drugs for over
30 years, and maintain a high quality of life.
*DISCLAIMER:
"The materials and information on this web site are intended to
provide general information for you. Please consult your physician on
specific medical questions. Do not use the information given on these
pages as a substitute for a physician consultation. All information
on this server is provided without warranty of any kind. Further, we
do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
currentness, or otherwise."
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Guaifenesin
- Fibromyalgia / Myofascial Pain Syndrome Medications
This is EXPERIMENTAL THERAPY.
Dr. Devin Starlanyl, MD
© Devin
Starlanyl, 1995-1998.
Guaifenesin (pronounced like "Gwhy-fen-es-in"),
is a medication often used to loosen phlegm and mucus in lungs. It has
been in use for over 20 years. R. Paul St. Amand M.D., an Internal Specialist,
Endocrinologist and professor at UCLA, a has discovered that it may
reverse the process of fibromyalgia. He suspects that one inherited
problem in FMS is a tendency toward a defect in phosphate excretion,
which ultimately causes an accumulation of phosphates within the mitochondria
(our cellular "chemical factories"). We're not sure of the
exact mechanism.
Guaifenesin
is the active ingredient in many cough medication expectorants. If possible,
use the pure guaifenesin (now only available in the USA in prescription
form), because the over-the-counter varieties have sugar and alcohol.
Store guaifenesin between 59 and 86 degrees F -- not in the refrigerator
or very warm room. You may become thirsty at first, and want to carry
some pure water around. Drink a lot of water. Guaifenesin will thin
your thick secretions, and help your body get rid of some wastes.
The
average starting dose is 300 mg twice a day, although some people who
are sensitive to medications may have to start at 300 mg a day. (If
you have reactive hypoglycemia as a perpetuating factor, you MUST be
on a balanced "Zone" diet for the reversal to take place.
(See "Mastering the Zone" by Barry Sears PhD for recipes and
information.) Dr. St. Amand has found less patients needing the diet
than I have, but his patients appear to be more sensitive to "blocking"
factors. Remember, we are trail-blazing here.) There will probably be
a period of flu-like fatigue as stored toxins and excess phosphates
start releasing. You should have a noticeable reaction in 3 to 10 days.
If you get no reaction, something is blocking the guaifenesin, you have
reactive hypoglycemia, or you need to raise the dosage to 600 mg twice
a day if tolerated. Your body is working hard during this time to process
wastes so that they can be excreted. After this, if needed, guaifenesin
dosage is generally raised 300 mgs a day at a time, after 10 days, until
the reversal begins. Map your pain patterns before starting this therapy,
and mark each area from 1 to 10 in pain intensity to help you monitor
therapy progression.
AVOID
SALICYLATE USE DURING GUAIFENESIN TREATMENT. SALICYLATES, FOUND IN MEDICATIONS
LIKE ASPIRIN, MANY HERBS AND TRILISATE WILL BLOCK THE BODY'S EFFORTS
TO EXCRETE EXCESS PHOSPHATES. If you use salicylate, the wastes are
liberated, but will circulate in the blood without being excreted. Large
quantities of herbs and herbal teas should be avoided -- many are rich
in salicylate. Small amounts of herbs for seasoning are acceptable.
Even aloe has salicylate. Every person has a different degree of sensitivity
to salicylate on guai. Some people are able to tolerate more than others
without guai being blocked. Many topical creams, such as some topical
rubs, sunscreens and cosmetics are salicylate-containing. Check with
your pharmacist. Many common medications such as Alka-Seltzer, Listerine
and Pepto-Bismol have salicylate.
Dr.
St. Amand has found three subsets in his practice. One group goes through
FMS reversal relatively quickly at 300 mg twice a day. They often feel
bad solidly until their symptoms clear suddenly. The largest subset
reverses at 600 mg twice a day. Another subset needs 1800 mg a day or
more, and just goes along slowly through the reversal process. Soon
you will get periods of time where symptoms ease. Often the reversal
is cyclical, with symptom-free periods interspersed with "cycling".
At least 40% of the people need more than 1600 mg a day. The calcium
excreted is limited to inappropriate calcium surplus. None of Dr. St.
Amand's patients have developed osteoporosis. Dr. St. Amand warns people
that guaifenesin therapy is "not for the faint of heart".
During the cycling you can have odd skin rashes, hair loss, burnt taste
in your mouth, pimples, gunky eyes, and an acidy smelling perspiration
unique to guaifenesin reversal (fortunately), and very strong-smelling,
acid urine. The urine gets very dark -- deep yellow, or even brown.
Vaginal secretions turn acidy, and can irritate. During guaifenesin
therapy, avoid adding a lot of phosphoric acid to your body. Colas are
loaded with it. It makes no sense to add a lot of phosphoric acid to
when your body is already working hard to get rid of its excess.
Reversal
signs and symptoms are NOT side-effects of guaifenesin. They are from
toxins and waste being released by the guai, and are a good sign, though
it won't feel like it. At least you'll understand why you often felt
"toxic". You were.
Headaches
are very common. Don't try to rush detox. It took a long time for your
body to get this sick. You can't clean it up overnight.
Sometimes
guai works on feeder deposits. These are large deposits which release
vast quantities of debris as these huge myofascial lumps dissolve. Your
body can only handle so much at one time. Excess debris forms temporary
deposits -- even on the teeth sometimes, until the body catches up processing
the wastes. Expect plateaus in the reversal process. Don't get discouraged.
We are all different. Allow your body to find the best pace. It will
eliminate the waste material as efficiently as it can. Meanwhile, do
whatever you can to help it. Drink lots of water, get as much rest as
you can, and avoid stress.
Knowing
that guai thins secretions and works at a cellular level, I think it
may partially work mechanically, cleaning off gummy cellular membranes.
Thinner secretions also allow more efficient breathing. I feel that
our reversal depends on the nature of our deposits: how many, how dense
they are, how much and what kind of tissue is displaced and how good
your body is at detoxifying. Also important is our electrolytic balance
-- we need balance for body maintenance, and to handle the disruption
caused by extra calcium phosphate (and who knows what else) release.
A good mineral supplement will help. This reversal process is not easy,
but neither is FMS/MPS. There's no way out but through.
Controlled
studies measure group response, not individual response, each of us
is unique. The only double-blinded study on FMS guaifenesin therapy
was done by Robert Bennett M.D. at Oregon Health Sciences University.
This study of 20 women showed guaifenesin equal to placebo. This response
is not uncommon when attempting to design experiments for old medications
with new usages. The study is flawed by no fault of Dr. Bennett, who
has done great things for "fibromites", nor of Dr. St. Amand,
who served as advisor to the study. We are only now discovering some
of the variables and fine-tuning treatment. This is experimental.
Point
1: The study was started before we knew the reversal does not take place
if reactive hypoglycemia is present. I have found that a little over
85% of the people I have seen with FMS have reactive hypoglycemia as
a perpetuating factor. We are talking of about 1000 patients. Some of
these with mild FMS "reversed" with the Zone diet alone. Of
those who tried guaifenesin (over 500), we are getting about 75 to 80
% drastic improvement. The others didn't stay with the therapy due to
the toxic-release effects or inability to follow the diet, except for
a less than 5% who did not get better. Some needed to delete colas from
their diet, since they took in as much phosphoric acid as was coming
out otherwise. Much of this therapy may depend on the acid/base balance
of the body. Nancy Medeiros (see the end of the chapter) is keeping
a running tally of Internet fibromites on guaifenesin therapy.
Point
2: All the patients in the study were given 600 mgs of guaifenesin twice
a day. Dr. St. Amand, an internist/endocrinologist and professor of
medicine at UCLA, has now found that only about 50% of patients respond
at this dosage, even these won't respond if they have reactive hypoglycemia.
FMS is not a condition that responds to "cookbook" medicine.
Point
3: Dr. St. Amand did not know about the blockage of guaifenesin by some
salicylate-containing herbs until September 1995. The study ended in
June 1995. Each of us has a varying tolerance of salicylate. Now that
I am "clearer" of whatever acids and materials come out on
"guai" therapy, I can tolerate cola now and then. I still
can't use stevia as a sugar substitute. Taking even a little of this
herb brings on the FMS achies.
Point
4: The response to guai is not a placebo response. Placebos do not result
in dark, smelly urine that cleans iron stains off the toilet bowl. Toilet
bowls do not respond to placebo effect. I have heard stories from fibromites
who years ago had been placed on guaifenesin therapy for asthma or upper
respiratory problems. They had to discontinue guai due to a "worsening"
of FMS symptoms, darkened urine etc. years before they heard of FMS
guai therapy. Patients who have been seen by Traditional Chinese Healers,
Naturopaths and other alternative specialists have reported that they
had been very toxic and acidic, but that they became "balanced"
on guaifenesin therapy.
Perhaps
the phosphoric and oxalic acids coming out in the urine (and dark "toxic
sweat") carry with them quinolinic acid. I. Jon Russell has found
that we create this toxin instead of serotonin in an alternate tryptophan
(kynurenine) metabolic pathway. We just don't know. Yet. Guai is not
a cure. But I have tried many remedies. Some have helped. Most have
not. I have seen many people given a new lease on life with guai, and
have experienced it myself, as has Dr. St. Amand. Others have enjoyed
periods of symptom remission.
With
most people, guaifenesin therapy seems to result in remission of symptoms.
This is not a cure. The symptoms will reappear if you overdo. We have
found that at least 50% of people with FMS have reactive hypoglycemia,
and need this. Otherwise you can be "reversed -- have all the tender
spots go away -- and you will still feel bad until you deal with the
hypoglycemia. You may never become symptom-free, because many symptoms
may be due to other processes, but you will be a lot more comfortable
until a cure can be found.
*DISCLAIMER:
"The materials and information on this web site are intended to
provide general information for you. Please consult your physician on
specific medical questions. Do not use the information given on these
pages as a substitute for a physician consultation. All information
on this server is provided without warranty of any kind. Further, we
do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
currentness, or otherwise."
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Guaifenesin
General Information
What is Guaifenesin?
Guaifenesin
is an expectorant, that is, a medication that promotes elimination of
mucus from the lungs. The expectorant effects of guaifenesin promote
elimination of mucous by thinning the mucous and lubricating the irritated
respiratory tract. Guaifenesin is an ingredient in many over-the-counter
cough and cold products. It is a safe medication
that may even be used by children. Derived from a tree bark extract
called guaiacum, it was first used to treat rheumatism during the 16th
century. Guaifenesin was first approved by the FDA in 1952. Twenty years
ago, the extract was synthesized, pressed into tablets and named guaifenesin.
Today, there are many formulations of guaifenesin available. Guaifenesin
is an expectorant with weakly uricosuric effects that has been shown
to effectively release phosphate and oxalate compounds from the body
through the urine. According to a survey of Dr. R. Paul St. Amand’s
patients, the administration of guaifenesin caused a 60 percent increase
in the excretion of phosphate, as well as a rise in both calcium and
oxalate excretion of up to 30 percent when taking guaifenesin.
How Does
Guaifenesin Work?
Dr. R. Paul St.
Amand, M.D., Assistant Clinical Professor of Endocrinology at Harbor-UCLA
believes guaifenesin therapy can significantly promote good health.
Dr. St. Amand’s theory of the medicinal effects of guaifenesin
is based on the premise that excess calcium and inorganic phosphate
compounds accumulate within cells to produce a state of hyperpermeability.
This condition allows excess fluids, ions and other unwanted substances
to flow into cell mitochondria, disrupting normal cell function, including
production of ATP, the body’s energy source. Dr. St. Amand believes
these factors cause the body to experience an energy deprived state,
in which widespread bodily functions are disrupted. Dr. St. Amand also
feels a possible genetic defect in some patients may be responsible
for the abnormality in natural phosphate excretion, thus resulting in
the buildup of these chemicals and subsequent symptoms.
A Note About
Fibromyalgia
Fibromyalgia (FM) is a chronic disorder characterized
by widespread musculoskeletal pain, tender points, and fatigue, and
according to the American College of Rheumatology, fibromyalgia affects
3 to 6 million Americans. It primarily occurs in women of childbearing
age, but children, the elderly, and men can also be affected. People
with this syndrome also experience sleep disturbances, morning stiffness,
irritable bowel, anxiety, depression and other symptoms.Treatment of
fibromyalgia requires a comprehensive approach. The physician, physical
therapist, and patient may all play an active role in the management
of fibromyalgia. There are many theories and treatments being discussed
and applied by different researchers and practitioners, but according
to one leading physician, guaifenesin is the most effective treatment
to date for reversing the effects of this debilitating disease.
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MEDICAL
INFORMATION
Guaifenesin
(oral)
(gwye FEN e sin)
Anti-Tuss, Bidex, Breonesin, Duratuss G, Fenesin, Ganidin NR, GG 200
NR, Guaifenesin LA, Guaifenex G, Guaifenex LA, Humibid L.A., Humibid
Pediatric, Liquibid, Muco-Fen 1200, Muco-Fen 800, Muco-Fen LA, Naldecon-EX
Senior, Organidin NR, Pneumomist, Q-Bid LA, Robitussin, Scot-Tussin,
Touro EX
What
is the most important information I should know about guaifenesin?
•
Drink plenty of extra fluids while you are taking this medication. Extra
fluids may help to relieve chest congestion.
• Do not crush or chew the tablets. Swallow them whole or break
them in half where they are scored to make them easier to swallow.
How is guaifenesin
commonly used and known?
• Guaifenesin
is an expectorant. Guaifenesin loosens phlegm and increases the lubrication
of your lungs allowing for a productive cough and decreased chest congestion.
• Guaifenesin is used to reduce chest congestion caused by the
common cold, infections, or allergies.
• Guaifenesin may also be used for purposes other than those listed
in this medication guide.
What should
I discuss with my healthcare provider before taking guaifenesin?
• Talk
to your doctor before taking guaifenesin if you have other medical conditions
or if you take other medicines.
• Guaifenesin is in the FDA pregnancy category C. This means that
it is not known whether guaifenesin will harm an unborn baby. Do not
take this medication without first talking to your doctor if you are
pregnant.
• It is also not known whether guaifenesin passes into breast
milk. Do not take this medication without first talking to your doctor
if you are breast-feeding a baby.
• Guaifenesin has not been approved by the FDA for use by children
younger than 2 years of age.
Pregnancy
• Although
one analysis found a correlation between guaifenesin use in the first
trimester and an increased risk of hernia in the fetus, others found
no increased risk of fetal malformations. Thus, guaifenesin should be
used in pregnancy only if the physician feels that the potential benefits
outweigh the potential and unknown risks.
How should
I take guaifenesin?
• Take
guaifenesin exactly as directed by your doctor. If you do not understand
these directions, ask your pharmacist, nurse, or doctor to explain them
to you.
• Take each dose with a full glass of water. Drink plenty of extra
fluids while you are taking this medication. Extra fluids may help to
relieve chest congestion.
• Take guaifenesin with food if it upsets your stomach.
• Do not crush or chew the tablets. Swallow them whole or break
them in half where they are scored to make them easier to swallow.
• The capsules may be swallowed whole, or they may be opened and
the contents sprinkled on soft food such as pudding or applesauce then
swallowed whole without crushing or chewing.
• To ensure that you get a correct dose, measure the liquid form
of guaifenesin with a special dose-measuring spoon or cup, not with
a regular table spoon. If you do not have a dose-measuring device, ask
your pharmacist where you can get one.
• Store guaifenesin at room temperature away from moisture, heat,
and direct sunlight.
What happens
if I miss a dose?
• Take
the missed dose as soon as you remember. However, if it is almost time
for your next dose, skip the missed dose and take only your next regularly
scheduled dose. Do not take a double dose of this medication.
What happens
if I overdose?
• An
overdose of guaifenesin is unlikely to occur. If you do suspect an overdose,
call an emergency room or poison control center near you.
What should
I avoid while taking guaifenesin?
•
Use caution when driving, operating machinery, or performing other hazardous
activities. Guaifenesin may cause dizziness. If you experience dizziness,
avoid these activities.
What are
the possible side effects of guaifenesin?
• No
serious side effects are expected from guaifenesin therapy. Stop taking
guaifenesin and seek emergency medical attention if you experience an
allergic reaction (difficulty breathing; closing of your throat; swelling
of your lips, tongue, or face; or hives).
• Other, less serious side effects may be more likely to occur.
Continue to take guaifenesin and talk to your doctor if you experience
· dizziness or headache,
· a rash, or
· nausea, vomiting, stomach upset, diarrhea, abdominal pain,
or drowsiness may occur.
• Side effects other than those listed here may also occur. Talk
to your doctor about any side effect that seems unusual or that is especially
bothersome.
What other
drugs will affect guaifenesin ?
• There
are no known interactions between guaifenesin and other medicines, although
the possibility exists. Talk to your doctor and pharmacist before taking
any prescription or over-the-counter medicines.
Dosing—
• The
dose of guaifenesin will be different for different patients. Follow
your doctor's orders or the directions on the label. The following information
includes only the average doses of guaifenesin. If your dose is different,
do not change it unless your doctor tells you to do so.
For
regular (short-acting) oral dosage forms (capsules, oral solution, syrup,
or tablets):
For cough:
Adults—200 to 400 milligrams (mg) every four hours.
Children
younger than 2 years of age—Use and dose must be determined by
your doctor.
Children 2 to 6 years of age—50 to 100 mg every four hours.
Children 6 to 12 years of age—100 to 200 mg every four hours.
For long-acting oral dosage forms (extended-release capsules or tablets):
For cough:
Adults—600 to 1200 mg every twelve hours.
Children younger than 2 years of age—Use is not recommended.
Children 2 to 6 years of age—300 mg every twelve hours.
Children 6 to 12 years of age—600 mg every twelve hours.
Where can
I get more information?
• Your
pharmacist has additional information about guaifenesin written for
health professionals that you may read.
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Improvement
of Cervical Factor with Guaifenesin
by Jerome H. Check,M.D., H.G Adleson, B.S.,
Chung-Hsis Wu, M.D.
Guaifenesin
is an expectorant capable of increasing respiratory tract fluid. It
is a common ingredient of many antitussive preparations. A study was
designed to see whether this agent could also improve cervical mucus,
as manifested by improved sperm survival and fertility.
Materials
and Methods
Forty couples with a minumum of 10 months of infertility
were selected where there was no sperm motility on postcoital testing.
Hostile cervical mucus rather than defective spermatogenesis was assumed
on the basis of accepting in the study only those couples where the
baseline spermogram after 48 hours abstinence had at least a count of
25 x 10 6/cc, a 2-cc volume, 70% motility, grade 3 of 4 quality, and
less than 20% abnormal forms.
The
postcoital test was performed on the 2nd day before the temperature
rise. Two baseline postcoital tests with no sperm motility 2 hours after
intercourse were required before the couple was entered in the study.
After wiping off the cervix with cotton, the mucus was aspirated with
a tuberculin syringe. If the mucus quality (spinn-barkeit, ferning,
lack of cellularity) was good but with no sperm motility, the couple
was not included in the study. Similarly, if cervical mucus was absent,
the couple was not accepted for the study.
Ovulation
was established on the basis of a serum progesterone level x2 over 10/ng/ml
taken 1 week before menses and a biphasic basal body temperature chart
with a minimum of a 13-day luteal phase. If drug therapy was required
to establish ovulation, the couple could be selected as long as the
drug required was not clomiphene citrate and/or human menopausal gonadotropins.
Each
woman was treated with 200mg guaifenesin orally three times daily from
day 5 to her temperature rise in either the commonly available antitussive
elixir form or in capsule form.
Response
to guaifenesin as reflected by postcoital evaluation was scored as "no
improvement" (no motile sperm), "marked improvement"
(at least 3 to 5 sperm per high-powered field with good linear progressive
motion), or "slight improvement" (some motile sperm but a
number or quality of motility inferior to standards set for the "marked
improvement" category). Mucus quality was judged before and after
guaifenesin as to spinnbarkeit and cellularity. If the patient showed
some improvement in the postcoital test, then the therapy was continued
for a minumum of 6 months unless conception occured first. If there
still was no sperm survival after two treatment cycles, the therapy
was considered a faliure and was stopped. Though the patient would then
be treated with other methods, as far as this study was concerned she
would only be listed in the "no improvement" category. No
patient in the study was allowed to have treatment with any other therapy
that could positively or negatively influence the cervical mucus.
The
tubal factor was investigated by either hysterosalpingogram or laparoscopy.
Seventy percent of the patients had a laparoscopy.
| |
Total |
Marked
Improvement |
Slight
Improvement |
No
Improvement |
| Number
of patients in Subgroup |
40 |
23
(57.5%) |
7
(17.5%) |
10
(25%) |
| I |
10 |
8 |
1 |
1 |
| II |
30 |
15 |
6 |
9 |
| Number
pregnant |
|
|
|
|
| I |
8 |
7 |
1 |
0 |
| II |
8 |
8 |
0 |
0 |
| %
pregnant |
|
|
|
|
| I |
80 |
87.5 |
100 |
0 |
| II |
26.6 |
53 |
0 |
0 |
| Total |
40 |
65.2 |
14.3 |
0 |
Results
The
response to guaifenesin is seen in Table 1. Twenty-three of 40 patients
showed marked improvement in postcoital following treatment, while 7
showed slight improvement was associated with improvement in the mucus
quality (improved spinnbarkeit and decreased cellularity).
Fifteen
pregnancies in 23 couples (65.2%) occurred in the group showing marked
improvement in the postcoital tests after guaifenesin therapy. One patient
with only a mild improvement in sperm survival achieved a pregnancy.
In ten patients with hostile mucus as the only detectable cause of the
infertility, eight became pregnant in an average 2.4 months. In the
remaining eight patients achieving pregnancies, where other fertility
problems coexisted, there was an average of 5.6 months of treatments
with guaifenesin. One patient, despite a marked improvement in sperm
survival and no other apparent cause for infertility, did not achieve
a pregnancy after 6 months of guaifenesin therapy. Only one of seven
patients showing a slight improvement in sperm survival achieved pregnancy.
The failure of eight patients to achieve pregnancices despite marked
improvement in sperm survival can be accounted for by other associated
fertility problems.
Discussion
The
results indicate that guaifenesin may improve cervical mucus and improve
fertility. A double-blind study was not deemed necessary, since it was
easy to follow the objective parameter of sperm survival and correlate
this with subsequent fertility. There is no evidence that psychological
factors can adversely affect cervical mucus in the presence of ovulation.
The exact mechanism of action of guaifenesin is not known, though it
would seem to be reasonably similar to its mechanism of improving respiratory
tract secretions. Other methods of treating the cervical factor have
been reviewed by Blasco. An additional technique employing high-dose
estrogen in combination with human menopausal gonadotropins has been
described more recently. The quoted pregnancy statistic following conventional
therapy of the cervical factor has been under 30%. With guaifenesin
therapy 40% of the entire cervical factor group conceived. In the subgroup
of patients whose fertility problem seemed likely to be related to the
cervical factor only, 80% conceived. These statistics will probably
improve when guaifenesin therapy is combined with other treatment modalities
for the cervical factor.
Fertility
and Sterility
May 1982
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specific medical questions. Do not use the information given on these
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do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
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Prevention
of recurrent HIV-associated Sinusitis
Name Of Substance Guaifenesin [USPD 1998; p. 348]
Accessed May 15, 2000.
Standard
Chemical Name 1,2-Propanediol, 3-(2-methoxyphenoxy).
Synonyms
Glycerol
guaiacolate
Glyceryl
guaiacyl ether
Guaiacol
glyceryl ether
Guaiphenesin
Methoxypropanediol
Glyceryl
guaiacolate
Guaiacyl
glyceryl ether
Protocol
ID Numbers Terminated NIAID ACTG 186
Pharmacological
Action
MODE OF ACTION:
Increases sputum and bronchial secretions by reducing
adhesiveness and surface tension. By reducing the viscosity of secretions,
guaifenesin increases the efficiency of the cough reflex and ciliary
action in removing accumulated secretions from the trachea and bronchi.
The drug is readily absorbed from the gastrointestinal tract and readily
metabolized and excreted in the urine. It has a plasma half-life of
1 hour. The major urinary metabolite is beta-(2-methoxyphenoxy) lactic
acid. In study that assessed changes in nasal symptoms among 23 HIV-infected
patients receiving either 3 weeks of guaifenesin (2400 mg daily) or
placebo, the guaifenesin group reported less nasal congestion and thinner
postnasal drainage. Guaifenesin appears to be effective in managing
HIV-infected patients with symptomatic rhinosinusitis. [PDR 1997; p
1605]
Diseases
Studied/treated Prevention of recurrent HIV-associated sinusitis. [Protocol
ID: ACTG 186 ] Classification Code Expectorant [USP DI 2000; p. 1659]
Other
Major Uses
Used
as expectorant in pharyngitis, bronchitis, and asthma. [PDR 1997; p
1605]
Substance
Interactions
May
interfere with laboratory test for diagnosis of carcinoid syndrome may
falsely elevate the VMA test for catechols. [PDR; 1997; p 1605]
Adverse
Effects
No
serious adverse effects have been reported with the use of guaifenesin.
Doses of guaifenesin larger than those required for expectorant action
may produce emesis, but GI upset at ordinary dosage levels is rare.
[PDR 1995; p 461]
Contraindications
Contraindicated in patients with hypersensitivity to guaifenesin. [PDR
1997; p 1605]
Chemical/physical
Data
MOLECULAR
FORMULA: C10-H14-O4
MOLECULAR
WEIGHT: 198.22 [USPD 1998; p. 348]
MELTING
POINT: 78.5-79 C [Merck Index 1996; p. 777]
ELEMENTAL
COMP: C60.59%, H7.12%, O32.29% [Merck Index 1996; p. 777]
SOLUBILITY:
Soluble in water, ethanol, chloroform, glycerol, propylene glycol, DMF
moderately soluble in benzene; practically insoluble in petroleum ether.
[Merck Index; 1996; p 777]
METHOD
OF DELIVERY: Oral. [AHFS Drug Information 1997; p 2092]
STORAGE
INSTRUCTIONS: Store at temperatures no greater than 30 C (86 F). Protect
from freezing. [Protocol ID: ACTG 186 ]
Management
of sinusitis in adult cystic fibrosis. Am J Rhinol. 1997 Jan-Feb;11(1):11-4.
MED/95140436. Friedman WH, Katsantonis GP, Bumpous JM.
Staging
of chronic hyperplastic rhinosinusitis: treatment strategies. Otolaryngol
Head Neck Surg. 1995 Feb;112(2):210-4. MED/95180023. Sisson JH, Yonkers
AJ, Waldman RH.
Effects
of guaifenesin on nasal mucociliary clearance and ciliary beat frequency
in healthy volunteers. Chest 1995 Mar;107(3):747-51. IPA/95. /1081197.
Wagner DL, Patel VS.
Steady-state
human pharmacokinetics and bioavailability of guaifenesin and pseudoephedrine
in a sustained-release tablet relative to immediate-release liquids.
Int J Pharm; VOL 114 ISS Feb 14 1995, P171-176, (REF 6). MED/95023331.
Brock MH, Dansereau RJ, Patel VS.
Use
of in vitro and in vivo data in the design, development, and quality
control of sustained-release decongestant dosage forms. Pharmacotherapy
1994 Jul-Aug;14(4):430-7. MED/93198678. Croughan-Minihane MS, Petitti
DB, Rodnick JE, Eliaser G.
Clinical
trial examining effectiveness of three cough syrups [see comments].
J Am Board Fam Pract 1993 Mar-Apr;6(2):109-15. MED/93023477. Wawrose
SF, Tami TA, Amoils CP.
The
role of guaifenesin in the treatment of sinonasal disease in patients
infected with the human immunodeficiency virus (HIV). Laryngoscope.
1992 Nov;102(11):1225-8. Entry Month 199212 Last Revision Date 20001107
Guaifenesin [USPD 1998; p. 348] - Guaifenesin [USPD 1998; p. 348]
----------------------------
Always watch for outdated information. ----------------------------
This
material is designed to support, not replace, the relationship that
exists between you and your doctor. This information is designed to
support, not replace, the relationship that exists between you and your
doctor.
*DISCLAIMER:
"The materials and information on this web site are intended to
provide general information for you. Please consult your physician on
specific medical questions. Do not use the information given on these
pages as a substitute for a physician consultation. All information
on this server is provided without warranty of any kind. Further, we
do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
currentness, or otherwise."

Interference
With Lab Tests
Guaifenesin can falsely elevate the results of laboratory
tests for vanillylmandelic acid (VMA), which is the main urinary metabolite
of catecholamines (adrenaline and noradrenaline). In addition, it is
well known that guaifenesin can cause false positive results in tests
for the serotonin metabolite, 5-hydroxyindoleacetic acid . You should
stop taking guaifenesin 48 hours before giving urine for either of these
tests.
By
the way, aspirin also interferes with VMA and 5-HIAA tests. Ephedrine
and caffeine cause increased values in 5-HIAA tests. Foods that are
high in serotonin (avocados, bananas, eggplant, pineapples, plums, and
tomatoes) can also cause false positives in 5-HIAA tests. An awful lot
of foods and even artifical coloring and flavoring can cause false positives
on a VMA test.
*DISCLAIMER:
"The materials and information on this web site are intended to
provide general information for you. Please consult your physician on
specific medical questions. Do not use the information given on these
pages as a substitute for a physician consultation. All information
on this server is provided without warranty of any kind. Further, we
do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
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WHAT
ARE SALYCILATES?
Salycilate
Sensitivity
Salicylate
sensitivity is the body's inability to handle more than a certain amount
of salicylates at any one time. A salicylate sensitive person may have
difficulty tolerating certain fruits, vegetables, or any products which
contain aspirin.
What Are
Salicylates?
Salicylates
are chemicals that occur naturally in many plants. They act as preservatives
to delay rotting and as protectants against harmful bacteria and fungi.
They are stored in the bark, leaves, roots, and seeds of plants. Salicylates
can be found naturally in some foods and its compounds are used in various
products.
Symptoms
of Intolerance
Salicylates sensitivity can manifest itself in many ways:
Anaphylaxis
(rare)
Asthma
Breathing difficulties
Changes in skin color
Congestion
Fatigue
Headaches
Hyperactivity
Itchy skin, rash, or hives
Itchy, watery, or swollen eyes
Lack of concentration or memory
Mouth ulcers or raw hot red rash around mouth
Nasal polyps
Persistent cough
Sinusitis
Some cognitive and perceptual disorders
Stomach aches or upsets
Swelling of eyelids, face, and lips
Swelling of hands and feet
Urgency to pass water or bedwetting
Wheezing
Sources of
Salicylates
Here is a list of products that may contain aspirin or salicylate compounds:
Acne
products
Breath savers
Bubble baths
Cosmetics
Fragrances and perfumes
Gums - mint flavored
Hair shampoos, conditioners, or sprays
Herbal remedies
Lipsticks
Lotions
Lozenges
Medications
Mouth washes
Muscle pain creams
Pain medications
Razors with aloe strips adjacent to the cutting edge
Shaving creams
Skin cleansers or exfoliants
Sun screens or tanning lotions
Supplements derived from rose hips or bioflavonoids
Topical creams
Toothpastes
Wart or callus removers
Watch Out
for These Terms
When reading labels be sure to also watch out for these terms:
Aspirin
Acetylsalicylic acid
Artificial food colorings
Artificial flavorings
Azo dyes
Benzoates (preservatives)
Benzyl salicylate
Beta-hydroxy acid
Choline salicylate
Disalcid
Ethyl salicylate
Isoamyl salicylate
Magnesium salicylate
Menthol
Methyl salicylate
Mint
Octylsalicylate
Peppermint
Phenylethyl salicylate
Salicylate
Salicylic acid
Salicylaldehyde
Salicylamide
Salsalate
Sodium salicylate
Spearmint
Salicylates
in Foods
Raw foods, dried foods, and juices contain higher levels
of salicylates than cooked food. The salicylate content in foods is
highest in unripened fruit and decreases as the fruit ripens. All fruit
and vegetables should be ripe and thickly peeled before eating. Salicylates
are often concentrated just under the skin of fruit and vegetables,
and in the outer leaves of vegetables.
The Feingold
Program
For those people who want to avoid salicylates and feel
overwelmed with the challenge, should take a few minutes to visit the
Feingold Association Web site. Shula Edelkind of the Feingold Association
(feingold.org) reports they do ongoing product information research.
She states, "All people have to do is use our Foodlist & Shopping
Guide. We have done the hard work for them. People can avoid the colorings,
flavorings and salicylates, and still have a 'normal' American diet
complete with fast food and junk food."
*DISCLAIMER:
"The materials and information on this web site are intended to
provide general information for you. Please consult your physician on
specific medical questions. Do not use the information given on these
pages as a substitute for a physician consultation. All information
on this server is provided without warranty of any kind. Further, we
do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
currentness, or otherwise."
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Guaifenesin
in the News
FDA orders most long-acting guaifenesin products off
market
Only
Adams' Mucinex product currently approved; other manufacturers have
until end of November to distribute 'illegal' products.
Last
October, FDA issued warning letters stating that single-ingredient extended-release
guaifenesin products are new drugs and require an approved new drug
application for legal marketing under the Federal Food, Drug, and Cosmetic
Act. The only approval, issued in July 2002, is for guaifenesin 600
mg extended-release tablets from Adams Laboratories.
In
the warning letters, sent to 66 manufacturers, FDA stated that its actions
"reflect the Agency's effort to maintain the necessary incentives
for companies to develop and submit to FDA scientific evidence to prove
the safety and effectiveness of marketed drug products."
FDA
also intends to publish a notice in the Federal Register about its policy
on unapproved drugs. In a talk paper posted to the FDA Web site, the
agency explained that it reviewed products in this category after approving
the Adams' product last July, and it concluded that products with unproven
safety and effectiveness should not remain on the market when an approved
product had become available. This preserves the incentives for companies
to develop and submit new drug applications, as required by law, FDA
added.
Guaifenesin's
main use is for productive coughs. It is the only FDA-approved nonprescription
expectorant. As a pre-1962 product, its effectiveness has never been
well established, but it causes few adverse effects and is commonly
included in many cough-and-cold products. As part of FDA's review of
OTC products, immediate-release guaifenesin was previously ruled to
be safe and effective.
NOTE:
Now in 2004 Guaifenesin in dosages of 600mg and below are ONLY available
Over The Counter (OTC)!
*DISCLAIMER:
"The materials and information on this web site are intended to
provide general information for you. Please consult your physician on
specific medical questions. Do not use the information given on these
pages as a substitute for a physician consultation. All information
on this server is provided without warranty of any kind. Further, we
do not warrant, guarantee, or make any representations regarding the
use, or the results in terms of correctness, accuracy, reliability,
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Treatment
of Fibromyalgia in Detail
Robert
Bennett MD, FRCP
If you are reading this you probably have a common syndrome of chronic
musculoskeletal pain called fibromyalgia. This chronic pain state is
now appreciated to be caused by abnormalities of sensory processing
within the spinal cord and brain. As such you will usually experience
a bewildering (both to you and your doctor) array of bodily and psychological
problems that can seldom be “cured”. However, armed with
both patience and knowledge, many fibromyalgia patients can be helped
to live with less pain and be more productive. In my own evolving experience
of dealing with this problem I can identify 7 aspects of management
that are of importance for your doctor to successful manage your fibromyalgia.
My Advice
to Doctors who care for Fibromyalgia Patients
1. Realize
that FM patients are going to be a chronic challenge.
2. Be non-judgmental
and prepared to be an advocate.
3. Understand
the pathophysiological basis for symptoms.
4. Analyze
and treat pain complaints in a systemic approach.
5. Recognize
and treat psychological problems at an early stage.
6. Recognize
associated syndromes of disordered sensory processing.
7. Involve
all FM patients in a program of stretching and gentle aerobic exercise.
Treatment
of pain in fibromyalgia
Pain is the
primary over-riding problem for most of you. Many of the problems you
experience are largely a secondary consequence of having chronic pain.
When pain is even partly relieved, fibromyalgia patients experience
a significant improvement in psychological distress, cognitive abilities,
sleep and functional capacity. A total elimination of pain is currently
not possible in the majority of fibromyalgia patients. However worthwhile
improvements can nearly always be achieved by a careful systematic analysis
of the pain complaints. As a generalization fibromyalgia related pain
can be divided into general pain (i.e. the chronic background pain experience
and focal pain (i.e. the intensification of pain in a specific region
– usually aggravated by movement). The latter is probably a potent
driving force in the generation of central sensitization. Attempts to
break the pain cycle, to enable patients to be more functional are especially
important. In general, most FM patients do not derive a great deal of
benefit from NSAID preparations or acetoaminophen, although NSAIDs are
very useful in the treatment of associated joint pain problems such
as osteoarthritis. Prednisone and other steroids have been shown to
be ineffective in the long term treatment of fibromyalgia.
General Pain.
The use of NSAIDs (e.g. ibuprofen, aspirin etc.) is usually disappointing;
it is unusual for FM patients to experience more than a 20% relief of
their pain, but many consider this to be worthwhile. Narcotics (propoxyphene,
codeine, and oxycodone) often provide a worthwhile relief of pain. In
most patients, concerns about addiction, dependency and tolerance are
ill founded. Ultram (Tramadol) and Ultracet (tramadol + Tylenol), are
the most useful pain medications in many patients. They both have the
advantages of having a low abuse potential and is not a prostaglandin
inhibitor; tramadol reduces the epileptogenic threshold and it should
not be used in patients with seizure disorders.
Currently
opiates are the most effective medications for managing most chronic
pain states (Friedman OP 1990, Portenoy 1996) . Their use is often condemned
out of ignorance regarding their propensity to cause addiction, physical
dependence and tolerance (Melzack 1990, Portenoy et al 1997, Wall 1997)
. While physical dependence (defined as a withdrawal syndrome on abrupt
discontinuation is inevitable) is inevitable, this should not be equated
with addiction (Portenoy 1996). Addiction is a dysfunctional state occurring
as a result of the unrestrained use of a drug for its mind-altering
properties; manipulation of the medical system and the acquisition of
narcotics from non-medical sources are common accompaniments. Addiction
should not be confused with "pseudo-addiction". This is a
drug-seeking behavior generated by attempts to obtain appropriate pain
relief in the face of under-treatment of pain. Opiates should never
be the first choice for pain relief in fibromyalgia, but they should
not be withheld if less powerful analgesics have failed. In my experience
many fibromyalgia patients want to try opioid medications, but then
give up on them due to unacceptable side effects, such as mental fog,
increased tiredness, dizziness, constipation and itching.
Local Pain.
Although you are experiencing widespread body pain -- a manifestation
of central sensitization -- you will also have multiple areas of tenderness
in muscles - so called "myofascial trigger points". The severity
of pain and the location of these "hot spots" typically varies
from month to month, and the judicious use of myofascial trigger point
injections and spray and stretch (see section on focal pain) is worthwhile
in selected patients. It is often worthwhile for your physician to identify
the most symptomatic points for myofascial therapy.
The steps
involved in the injection of trigger points are:
1. Accurate
identification of the trigger point.
2. Identification
and elimination of aggravating factors.
3. The precise
injection of the myofascial trigger points with 1% procaine (a local
anesthetic).
4. Passive
stretching of the involved muscle after the local anesthetic has taken
effect; this is
often aided by spraying the overlying skin with an ethyl chloride spray.
In most FM
patients, this myofascial therapy needs to be repeated over a period
of several weeks and occasionally over several months. Unresponsiveness
is usually due to failure to eliminate an aggravating factor, imprecise
injection of the trigger point, or failure to inject satellite trigger
points. Trigger points are usually injected with 3 to 5 ml of 1-% procaine.
Please note that these are not “steroid shots”.
Performing
“myofascial spray and stretch” often enhances the efficacy
of trigger point injections immediately after the injections. Spray
and stretch consists of an application of a vapocoolant spray, such
as ethyl chloride over the muscle with simultaneous passive stretching.
A fine stream of the spray is aimed toward the skin directly overlying
the muscle with the active trigger point. A few sweeps of the spray
are passed over the trigger point and the zone of reference. This is
followed by a progressively increasing passive stretch of the muscle.
Evaluation
by an occupational and physical therapist often provides worthwhile
advice on improved ergonomics, biomechanical imbalance and the formulation
of a regular stretching program. Hands-on physical therapy treatment
with heat modalities is reserved for major flares of pain, as there
is no evidence that long-term therapy alters the course of the disorder.
The same comments can be made for acupuncture, TENS units and various
massage techniques.
Treatment
of Sleep Disorders.
Non-restorative sleep is a problem for most of you and contributes to
your feelings of fatigue and seems to intensify their experience of
pain. Effective management involves (1) ensuring an adherence to the
basic rules of sleep hygiene, (2) regular low grade exercise, (3) adequate
treatment of associated psychological problems (depression, anxiety
etc.) and (4) the prescription of low dose tricyclic antidepressants
(amitryptiline, trazadone, doxepin, imipramine etc. Some fibromyalgia
patients cannot tolerate TCAs due to unacceptable levels of daytime
drowsiness or weight gain. In these patients benzodiazopine-like medications
such as Ambiem (zolpidem) are usually very useful. Some fibromyalgia
patients suffer from a primary sleep disorder, which requires specialized
management. About 25% of male and 15% of female fibromyalgia patients
have sleep apnea. Unless specific questions about this possibility are
asked sleep apnea will often be missed. Patients with sleep apnea usually
require treatment with positive airway pressure (CPAP) or surgery. By
far the commonest sleep disorder in fibromyalgia patients is restless
leg syndrome. This can be effectively treated with L-Dopa/carbidopa
(Sinemet 10/100 mg at suppertime) or clonazepam (Klonipin 0.5 or 1.0
mg at bedtime).
Exercise
for Fibromyalgia Patients
Fibromyalgia
patients cannot afford not to exercise as deconditioned muscles are
more prone to microtrauma and inactivity begets dysfunctional behavioral
problems . However, musculoskeletal pain and severe fatigue are powerful
conditioners for inactivity. All fibromyalgia patients need to have
a home program with muscle stretching and gentle strengthening, and
aerobic conditioning. There are several points that need to be stressed
about exercise in FM patients: (i) Exercise is health training, not
sport’s training. (ii) Exercise should be non-impact loading.
(iii) Aerobic exercise should be done for 30 minutes each day. This
may be broken down into three 10 minute periods or other combinations,
such as two 15 minute periods, to give a cumulative total of 30 minutes.
This should be the aim -- it may take 6-12 months to achieve this level.
(vi) Strength training should emphasize on concentric work and avoid
eccentric muscle contractions. (vii) Regular exercise needs to become
part of the usual lifestyle; it is not merely a 3-6 month program to
restore them to health. Suitable aerobic exercise includes: regular
walking, the use of a stationery exercycle or Nordic track (initially
not using the arm component). Patients who are very deconditioned or
incapacitated should be started with water therapy using a buoyancy
belt (Aqua-jogger).
Recognition
and treatment of psychological distress
As you suffer
from chronic pain there is a distinct possibility that you may develop
secondary psychological disturbances, such as depression, anger, fear,
withdrawal and anxiety. When “an event” is associated with
the onset of the fibromyalgia you may adopt the role of a "victim".
Sometimes these secondary reactions become the "major problem"
for some patients. The prompt diagnosis and treatment of these secondary
features is essential to effective overall management of fibromyalgia
patients. Some fibromyalgia patients develop a reduced functional ability
and have difficulty being competitively employed. In such cases your
doctor will hopefully act as an advocate in sanctioning a reduced or
modified load at work and at home. Unless you have a severe psychiatric
illness (e,g, major depressive illness or a psychosis), referral to
psychiatrists is usually non-productive. Psychological counseling, particularly
the use of techniques such as cognitive restructuring and biofeedback,
may benefit some patients who are having difficulties coping with the
realities of living with their pain and associated problems.
Fibromyalgia
associated syndromes
It is not
unusual for fibromyalgia patients to have an array of bodily complaints
other than musculoskeletal pain. It is now thought that these symptoms
are a result of the abnormal sensory processing – as described
in the previous section. Recognition and treatment of these associated
problems are important in the overall management of your fibromyalgia.
Non-restorative
sleep
Cognitive dysfunction
Chronic fatigue
Cold intolerance
Restless leg syndrome
Multiple sensitivities
Irritable bowel syndrome
Dizziness
Irritable bladder syndrome
Neurally mediated hypotension
1. Chronic
fatigue: The common treatable cause of chronic fatigue in fibromyalgia
patients are: (1) inappropriate dosing of medications (TCAs, drugs with
antihistamine actions, benzodiazapines etc.), (2) depression, (3) aerobic
deconditioning, (3) a primary sleep disorder (e.g. sleep apnea), (4)
non-restorative sleep (see above) and (5) neurally mediated hypotension
(see below). A new drug called Provigil is of some help when used intermittently
for management of fatigue.
2. Restless
leg syndrome: This strictly refers to daytime (usually maximal in the
evening) symptoms of (1) unusual sensations in the lower limbs (but
can occur in arms or even scalp) that are often described as paresthesia
(numbness, tingling, itching, muscle crawling) and (2) a restlessness,
in that stretching or walking eases the sensory symptoms. This daytime
symptomatology is nearly always accompanied by a sleep disorder - now
referred to as periodic limb movement disorder (formerly nocturnal myoclonus).
Treatment is simple and very effective – DOPA / Levodopa (Sinemet)
in an early evening dose of 10/100 (a minority require a higher dose
or use of the long acting preparations).
3. Irritable
bowel syndrome: This common syndrome of GI distress that occurs in about
20% of the general population is found in about 60% of fibromyalgia
patients. The symptoms are those of abdominal pain, distension with
an altered bowel habit (constipation, diarrhea or an alternating disturbance).
Typically the abdominal discomfort is improved by bowel evacuation.
Due to abnormal sensory processing these symptoms may be quite distressing
to fibromyalgia patients. Treatment involves (1) elimination of foods
that aggravate symptoms, (2) minimizing psychological distress, (3)
adhering to basic rules for maintaining a regular bowel habit, (4) prescribing
medications for specific symptoms; constipation (stool softener, fiber
supplementation and gentle laxatives such as bisacodyl), diarrhea (loperamide
or diphenoxylate) and antispasmodics (dicyclomine or anticholinergic
/ sedative preparations such as Donnatal).
4. Irritable
bladder syndrome: This is found in 40-60% of fibromyalgia patients.
The initial incorrect diagnoses are usually recurrent urinary tract
infections, interstitial cystitis or a gynecological condition. Once
these possibilities have been ruled out a diagnosis of irritable bladder
syndrome (also called female urethal syndrome) should be considered.
The typical symptoms are those of suprapubic discomfort with an urgency
to void, often accompanied by frequency and dysuria. In a sub-population
of fibromyalgia patients this is related to a myofascial trigger point
in the pubic insertion of the rectus abdominus muscles – and may
be helped by a procaine myofascial trigger point injection). Treatment:
involves (1) increasing intake of water, (2) avoiding bladder irritants
such as fruit juices (especially cranberry), (3) pelvic floor exercises
(e.g. Kagel exercises) and the prescription of antispasmodic medications
(e.g. oxybutinin, flavoxate, hyoscamine).
5. Cognitive
dysfunction: This is a common problem for many fibromyalgia patients.
It adversely affects the ability to be competitively employed and may
cause concern as to an early dementing type of neurodegenerative disease.
In practice the latter concern has never been a problem and patients
can be reassured. The cause of poor memory and problems with concentration
is, in most patients, related to the distracting effects of chronic
pain and mental fatigue. Thus the effective treatment of cognitive dysfunction
in fibromyalgia is dependent on the successful management of the other
symptoms.
6. Cold intolerance:
About 30% of fibromyalgia patients complain of cold intolerance. In
most cases this amounts to needing warmer clothing or turning up the
heat in their homes. Some patients develop a true primary Raynaud’s
phenomenon (which may mislead an unknowing physician to consider diagnoses
such as SLE or scleroderma. Many fibromyalgia patients have cold hands
and feet, and some have cutis marmorata (a lace like pattern of violaceous
discoloration of their extremities on cold exposure). Treatment involves:
(1) keeping warm, (2) low-grade aerobic exercise (which improves peripheral
circulation), (3) treatment of neurally mediated hypotension (see below),
and (4) the prescription of vasodilators such as the calcium channel
blockers (but these may aggravate the problem in-patients with hypotension).
7. Multiple
sensitivities: One result of disordered sensory processing is that many
sensations are amplified in fibromyalgia patients. In general fibromyalgia
patients are less tolerant of adverse weather, loud noises, bright lights
and other sensory overloads. Treatment involves being aware that this
is a fibromyalgia-related problem and employing avoidance tactics.
8. Dizziness:
Is a common complaint of fibromyalgia patients. Before this symptom
is attributable to fibromyalgia a thorough for other causes should be
pursued (e.g. postural vertigo, vestibular disorders, 8th nerve tumors,
demyelinating disorders, brain stem ischemia and cervical myelopathy).
In many cases no obvious cause is found, despite sophisticated testing.
Treatable causes related to fibromyalgia include: (1) proprioceptive
dysfunction secondary to muscle deconditioning, (2) proprioceptive dysfunction
secondary to myofascial trigger points in the sterno-cleido-mastoids
and other neck muscles, (3) Neurally mediated hypotension (see below)
and (4) medication side effects. Treatment is dependent on making an
accurate diagnosis. In patients in whom no obvious cause is found a
trial of physical therapy, concentrating on proprioceptive awareness
may prove worthwhile.
9. Neurally
mediated hypotension: Patients with this problem usually have a low
blood pressure that does not go up normally on standing or on exercise.
Although such patients often have a low ambient BP with postural changes,
these findings are not a prerequisite for diagnosis. A tilt table test
with the infusion of isproterenol is the most reliable way to confirm
this diagnosis. Treatment involves: (1) education as to the triggering
factors and their avoidance, (2) increasing plasma volume (increased
salt intake, prescription of florinef), (3) avoidance of drugs that
aggravate hypotension (e.g. TCA’s, anti-hypertensives), (4) prevent
reflex (prescribe ß-adrenergic antagonists or disopyramide) and
(5) minimize the efferent limb of the reflex (prescribe a2-adrenergic
agonists or anti-cholinergic agents).
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Cognitive
Therapy - What is it and how does it help?
by
Carol Burckhardt Ph.D
All
comprehensive fibromyalgia (FM) treatment programs include non-drug
components such as cognitive-behavioral treatment. This broad treatment
area emphasizes the relationship between thoughts, beliefs, emotions
and behavior. In fact, it assumes that thoughts are powerful determiners
of how we feel and behave and that altering maladaptive thought patterns
will result in desirable behavior changes. Cognitive strategies include
education in recognizing thought patterns that are maladaptive along
with learning and practice of specific techniques for decreasing distress,
pain, fatigue, and anxiety. Cognitive therapy contains 4 components:
(1) coping skills training, (2) self-control training, (3) problem-solving
skills training, and (4) cognitive restructuring methods. Although I
have found that most people with FM already engage in a number of positive
coping strategies, are ready to learn relaxation strategies and able
to develop better ways to solve problems, when approaching the area
of cognitive restructuring some people respond skeptically.
“Oh,
here we go again! Just thinking positively doesn’t take my symptoms
away.”
“If
I change the way I think about my pain and my pain decreases, people
(my
family, my work colleagues, my doctor) are going to believe that fibromyalgia
is ‘all
in my head.’”
“What
am I supposed to do, try to fool myself into believing that things are
different?”
Let’s
explore cognitive restructuring with the goal of understanding better
what it is and what it isn’t and what its potential is for helping
people with FM manage their symptoms better.
Have you
ever worried about anything? Have you ever felt your body relax when
someone said a kind word to you? If so, you have experienced the intimate
connection between thoughts and feelings. Think about it, when you worry
your body responds with sensations of anxiety (knots in your stomach,
increased heart rate, sweaty palms, insomnia). Yet, the negative things
you are worrying about aren’t actually happening at the time that
you are worrying. They are happening only in your thoughts. On the positive
side, if someone says, “I’m really sorry that you are in
so much pain,” or, “I want to help in any way I can,”
you may feel your muscles relax, your stomach stop churning, and your
breathing become less shallow. Again, these body reactions happen even
though the helper only said something to you. She didn’t massage
your muscles, give you a Zantac or even tell you to breathe deeply.
If you want to try out this connection in a simple way, think about
eating a lemon or savoring a piece of Godiva chocolate and see what
happens. Bet you start to salivate. What I’m trying to convince
you of is that a very powerful connection exists between how you think,
how you perceive messages from yourself and others, and how you feel
both emotionally and physically.
These ongoing
thoughts are the little voice in your head that babbles to you all the
time. Sometimes people I see in counseling aren’t aware that they
are constantly engaged in a running automatic dialog. If that seems
to be the case, I ask them to spend the next week listening to themselves.
Invariably, they come back with all sorts of tales that their conscious
mind has been telling them. This cognitive part is always actively evaluating,
rationalizing, scheming, analyzing and distorting reality at times.
Have you ever said something and then wondered, “Why did I say
that?” followed by, “That was a dumb thing to say.”
Or maybe your neighbor brought over a plate of freshly baked cookies.
You smiled, thanked her and felt both a little happy and a little sad.
Then you realized that your thoughts were centering around, “She
probably thinks I can’t cook. I look like such a mess and my house
is a disaster. I’m just inadequate.”
All people
engage in cognitive distortions from time to time. Some very common
negative thoughts that people with FM have include:
“Why
me?” Life isn’t fair.”
“My
pain will never get better.”
“I
shouldn’t ask for help.”
“No
one understands me.”
What cognitive
restructuring focuses on is helping you to identify the long-standing
patterns of automatic thinking associated with unhappiness, anxiety,
depression, and physical symptoms. Once these patterns are identified,
you can decide if you wish to change them. In other words, cognitive
restructuring is an active, individual process that you control. A good
therapist serves as a guide to the process, often asking questions such
as,
“Can
you think of an alternative way to view this situation?”
“Is
believing that you are worthless helpful to you?”
“Is
your pain always this bad?”
“Who
told you that you should ______?”
Sometimes
she/he might suggest a different label like,
“Instead
of seeing yourself as a martyr, maybe you could think of yourself as
a
nurturer.”
“Maybe
instead of telling yourself that you should do something, you could
ask
yourself if you want to do it.”
These questions
and suggestions are meant to help you reframe or restructure your thoughts
into more realistic and helpful thoughts. As these new thoughts and
belief become more a part of you, they won’t feel foreign or feigned.
For example, reframing the belief that life isn’t fair into, “perhaps
that is true, but believing and telling myself that doesn’t help
me feel any better; instead I will tell myself that living my life to
the fullest is more important than being frustrated about whether it
is fair,” is likely to change your emotional state from one of
depression and anger to one of peace and joy. As the ancient writer
of Proverbs said, “ A depressed spirit saps one’s strength
but a happy mind is good medicine.(17:22) ”
First
published in The Fibromyalgia Times, 3(3), 14-15, 1998
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Fibromyalgia
in Frida Kahlo's life and art
The
great Mexican painter Frida Kahlo (1907-1954) is without doubt one of
the most intense and emotive artists of the twentieth century. Frida's
life changed dramatically at the age of 18, when she was involved in
a terrible accident. A streetcar violently impacted the bus in which
she was riding. She suffered multiple bone fractures, including the
third and fourth lumbar vertebrae, and had a deep abdominal wound inflicted
by a metal rod. She was confined for several months in a plaster corset.
From that time on, Frida suffered severe, widespread pain and profound
fatigue. Generalized pain and exhaustion lingered with her for the remainder
of her life.
Through the
years, a variety of diagnoses were offered to explain her chronic illness,
such as tuberculosis and syphilis, that were later ruled out. She received
diverse types of treatments, including medications and long periods
of confinement in a metal or plaster corset. In efforts to relieve her
pain, she underwent several orthopedic operations on her spine, both
in Mexico and in the United States, without improvement in her symptoms.
Despite her
debilitating illness, Frida was engaged in an active social life. She
had a tempestuous marriage to the famous Mexican muralist Diego Rivera.
She traveled extensively and had relationships with the world leaders
and artistic personalities of her time. Frida began painting after her
accident. During periods of immobilization in a plaster corset, she
used a special easel, and a mirror was attached to the canopy of her
bed so that she could focus on herself. Although her painting skills
were largely self-taught, she was also acquainted with the traditional
schools of painting. Both in her oeuvre and in her customs, she looked
back with devotion to her Mexican roots. The Surrealists claimed her
as one of their own. The stillness of her self-portraits reflects the
influence of her father, who was a photographer.
Frida used
to describe her own paintings as "the most frank expression of
myself". Her self-portraits are impassioned. Anguish and pain are
the common themes of her work. These emotions are dramatically expressed
in her oil painting, "The Broken Column (see picture on left).
As Hayden Herrera observed, Frida's determined impassivity creates an
almost unbearable tension. Pain is made vivid by nails driven into her
naked body. A gap resembling an earthquake fissure splits her torso.
The opened body suggests surgery. Inside her torso, we see a cracked
ionic column. The corset's white straps accentuate her beautiful body.
Her hips are wrapped in a cloth suggestive of Christian martyrdom. She
stares straight ahead with dignity. Tears dot her cheeks, but her features
refuse to cry. An immense and barren plain in the background conveys
physical and emotional suffering.
To explain
Frida's chronic illness, we offer an alternative diagnosis. Our opinion
is that she suffered posttraumatic fibromyalgia. This prevalent syndrome
is characterized by persistent widespread pain, chronic fatigue, sleep
disorders, and vegetative symptoms, and by the presence of tender points
in well-defined anatomic areas. The concept of fibromyalgia as a clinical
entity as we know it today was probably unknown to most physicians of
the early twentieth century. Our diagnosis explains her chronic, severe,
widespread pain accompanied by profound fatigue. It also explains the
lack of response to diverse forms of treatment. The onset of fibromyalgia
after physical trauma is well-recognized.
A drawing
in Frida's diary reinforces our diagnostic impression. She depicts herself
in pain, and 11 arrows point to anatomic sites that are near the conventional
fibromyalgia tender points. Of course, because fibromyalgia is an illness
without anatomic sequelae, our contention cannot be proven or disproven.
What appears certain is that Frida's self-portraits convey widespread
pain and anguish with the emotional overtones that fibromyalgia patients
frequently use to describe their illness.
We are indebted
to Dr. Leonardo Zamudio, who allowed us to have access to Frida Kahlo's
medical records, to Ms Dolores Olmedo, who gave permission to reproduce
"The Broken Column," and to Dr. Robert Kalish, who kindly
reviewed the manuscript.
Manuel Martinez-Lavin,
MD, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico
Mary-Carmen
Amigo, MD, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico
City, Mexico
Javier Coindreau,
MD, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico
Juan Canoso,
MD, American British Cowdray Hospital, Mexico City, Mexico
REFERENCES
1.
Herrera H. Frida: a biography of Frida Kahlo. New York: Harper Row;
1983.
2. Tibol
R. Frida Kahlo: una vida abierta. Mexico City: Universidad Nacional
Autonoma de Mexico; 1998.
3. Zamora
M. Frida Kahlo: the brush of anguish. San Francisco: Chronicle Books;
1990.
4. Monsivais
C. Vazquez-Bayod R. Frida Kahlo: una vida, una obra. Mexico City: Conaculta;
1992.
5. Del Conde
T. Frida Kahlo: la pintora y el mito. Mexico City: Universidad Nacional
Autonoma de Mexico; 1992.
6. Wolfe
F, Smythe HA, Yunus MB, Bennett RM, Bombardier C, Goldenberg DL, et
al. The American College of Rheumatology 1990 criteria for the classification
of fibromyalgia: report of the multicenter criteria committee. Arthritis
Rheum 1990; 33:160-72.
7. Martinez-Lavin
M, Hermosillo AG, Rosas M, Soto M-E. Circadian studies of autonomic
nervous balance in patients with fibromyalgia: a heart rate variability
analysis. Arthritis Rheum 1998; 41:1966-71.
8. Buskila
D, Neumann L, Vaisberg G, Alkalay D, Wolfe F. Increased rate of fibromyalgia
following cervical spine injury: a controlled study of 161 cases of
traumatic injury. Arthritis Rheum 1997; 40:446-52.
9. Freeman
P. Frida Kahlo: Diario: autorretrato intimo. Mexico City: La Vaca Independiente;
1995.
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MORE
GUAIFENESIN MEDICAL INFORMATION
WHY
IS THIS MEDICATION ORDINARILY PRESCRIBED?
Guaifenesin
is used to relieve chest congestion . Guaifenesin may help control symptoms
but does not treat the cause of symptoms or speed recovery. Guaifenesin
is in a class of medications called expectorants. It works by thinning
the mucus in the air passages to make it easier to cough up the mucus
and clear the airways.
How
should this medicine be used?
Guaifenesin
comes as a tablet, a capsule, an extended-release (long-acting) tablet,
dissolving granules, and a syrup (liquid) to take by mouth. The tablets,
capsules, dissolving granules, and syrup are usually taken with or without
food every 4 hours as needed. The extended-release tablet is usually
taken with or without food every 12 hours. Follow the directions on
the package or on your prescription label carefully, and ask your doctor
or pharmacist to explain any part you do not understand. Take guaifenesin
exactly as directed. Do not take more or less of it or take it more
often than prescribed by your doctor.
Guaifenesin
comes alone and in combination with antihistamines, cough suppressants,
and decongestants. Ask your doctor or pharmacist for advice on which
product is best for your symptoms. Check nonprescription cough and cold
product labels carefully before using two or more products at the same
time. These products may contain the same active ingredient(s) and taking
them together could cause you to receive an overdose. This is especially
important if you will be giving cough and cold medications to a child.
Nonprescription
cough and cold combination products, including products that contain
guaifenesin, can cause serious side effects or death in young children.
Do not give these products to children younger than 4 years of age.
If you give these products to children 4 to 11 years of age, use caution
and follow the package directions carefully.
If you are
giving guaifenesin or a combination product that contains guaifenesin
to a child, read the package label carefully to be sure that it is the
right product for a child of that age. Do not give guaifenesin products
that are made for adults to children.
Before you
give a guaifenesin product to a child, check the package label to find
out how much medication the child should receive. Give the dose that
matches the child's age on the chart. Ask the child's doctor if you
don't know how much medication to give the child.
If you are
taking the liquid, do not use a household spoon to measure your dose.
Use the measuring spoon or cup that came with the medication or use
a spoon made especially for measuring medication.
Swallow the
extended-release tablets whole with a full glass of water. Do not break,
crush, or chew them.
If you are
taking the dissolving granules, empty the entire contents of the packet
onto your tongue and swallow.
If your symptoms
do not improve within 7 days or if you also have a high fever, a rash,
or a headache that does not go away, call your doctor.
Other
uses for this medicine
This medication
is sometimes prescribed for other uses; ask your doctor or pharmacist
for more information.
What
special precautions should I follow?
Before taking guaifenesin,
* tell your
doctor and pharmacist if you are allergic to guaifenesin, any other
medications, or any of the ingredients in the guaifenesin product you
plan to take. Check the package label for a list of the ingredients.
* tell your doctor and pharmacist what prescription and nonprescription
medications, vitamins, nutritional supplements, and herbal products
you are taking or plan to take.
* tell your doctor if you smoke and if you have or have ever had a cough
that occurs with a large amount of phlegm (mucus) or if you have or
have ever had a breathing problem such as asthma, emphysema, or chronic
bronchitis. If you will be taking the dissolving granules, tell your
doctor if you are on a low magnesium diet or if you have kidney disease.
* tell your doctor if you are pregnant, plan to become pregnant, or
are breast-feeding. If you become pregnant while taking guaifenesin,
call your doctor.
* if you have phenylketonuria (PKU, a inherited condition in which a
special diet must be followed to prevent mental retardation), you should
know that the dissolving granules may be sweetened with aspartame, a
source of phenylalanine.
What special
dietary instructions should I follow?
Return to top
Drink plenty
of fluids while you are taking this medication.
Unless your
doctor tells you otherwise, continue your normal diet.
In case of
overdose, call your local poison control center at 1-800-222-1222. If
the victim has collapsed or is not breathing, call local emergency services
at 911.
What
other information should I know?
Ask your
pharmacist any questions you have about guaifenesin.
It is important
for you to keep a written list of all of the prescription and nonprescription
(over-the-counter) medicines you are taking, as well as any products
such as vitamins, minerals, or other dietary supplements. You should
bring this list with you each time you visit a doctor or if you are
admitted to a hospital. It is also important information to carry with
you in case of emergencies.
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BRAND
NAMES FOR GUAIFENESIN
* Albatussi®n
EX
* Bidex®
* Buckley's® Chest Congestion
* Diabetic Tussin® EX
* Fenesin® IR
* Ganidin® NR
* Genatuss®
* Glytuss®
*
Guai-Aid®
* Guaiatussin®
* Guaifen® NR
* Guiacough®
* Guiatuss®
* Halotussin®
* Humibid®
E
* Hytuss®
* Liquibid®
* Lotussin®
* Mallotuss®
* Mastussin®
* Miltuss® EX
* Mucinex®
* Mytussin®
* Naldecon-EX®
* Orgadin®
* Organidin® NR
* Phanasin®
* Q-Tussin®
* Ri-Tussin®
* Robafen®
* Robichem®
* Robitussin®
* Scot-Tussin®
* Siltuss® DAS
* Siltussin®
* SoloGuai®
* Sorbutuss®
* T-Tussin®
* Tusscidin®
* Tussin®

Brand
names of combination products:
*
AccuHist® PDX (containing Brompheniramine, Dextromethorphan, Guaifenesin,
Phenylephrine)
* Albatussin® PE (containing Guaifenesin, Phenylephrine)
* Benylin® Expectorant (containing Dextromethorphan, Guaifenesin)
* Betavent® (containing Carbetapentane, Guaifenesin)
* Bitex® (containing Codeine, Guaifenesin)
* Bromhist® PDX (containing Brompheniramine, Dextromethorphan, Guaifenesin,
Phenylephrine)
* Broncholate® (containing Ephedrine, Guaifenesin)
* Brondil® (containing Dyphylline, Guaifenesin)
* Bronkaid® (containing Ephedrine, Guaifenesin)
* Bronkotuss® (containing Chlorpheniramine, Ephedrine, Guaifenesin)
* Brontex® (containing Codeine, Guaifenesin)
* Carbatuss® (containing Carbetapentane, Guaifenesin, Phenylephrine)
* Carbetaplex® (containing Carbetapentane, Guaifenesin, Phenylephrine)
* Cheracol® D (containing Dextromethorphan, Guaifenesin)
* Cheracol® with Codeine (containing Codeine, Guaifenesin)
* Cheratussin® (containing Codeine, Guaifenesin)
* Codafen® (containing Codeine, Guaifenesin)
* Codiclear® DH (containing Guaifenesin, Hydrocodone)
* Comtrex® Deep Chest Cold Non Drowsy (containing Acetaminophen,
Guaifenesin)
* Coricidin® HBP Chest Congestion (containing Dextromethorphan,
Guaifenesin)
* Deconex® (containing Guaifenesin, Phenylephrine)
* Difil® G (containing Dyphylline, Guaifenesin)
* Dilaudid® Cough (containing Guaifenesin, Hydromorphone)
* Dilex-G® (containing Dyphylline, Guaifenesin)
* Dilor-G® (containing Dyphylline, Guaifenesin)
* Donatuss DC® (containing Dihydrocodeine, Guaifenesin, Phenylephrine)
* Donatussin® (containing Chlorpheniramine, Dextromethorphan, Guaifenesin,
Phenylephrine)
* Drituss® DM (containing Dextromethorphan, Guaifenesin)
* Duratuss® DM (containing Dextromethorphan, Guaifenesin)
* Dyfilin® GG (containing Dyphylline, Guaifenesin)
* Dyflex-G® (containing Dyphylline, Guaifenesin)
* Dyphysin® (containing Dyphylline, Guaifenesin)
* Endacof® XP (containing Guaifenesin, Hydrocodone)
* Entuss® (containing Guaifenesin, Hydrocodone)
* Gentex® HC (containing Guaifenesin, Hydrocodone, Phenylephrine)
* Gentex® LQ (containing Carbetapentane, Guaifenesin, Phenylephrine)
* Glycotuss-DM® (containing Dextromethorphan, Guaifenesin)
* Guaifen® DM (containing Dextromethorphan, Guaifenesin)
* Guiatussin® DM (containing Dextromethorphan, Guaifenesin)
* Halotussin® DM (containing Dextromethorphan, Guaifenesin)
* Humibid® CS (containing Dextromethorphan, Guaifenesin)
* Hycotuss® (containing Guaifenesin, Hydrocodone)
* Kwelcof® (containing Guaifenesin, Hydrocodone)
* Levall® (containing Carbetapentane, Guaifenesin, Phenylephrine)
* Lotussin® DM (containing Dextromethorphan, Guaifenesin)
* Lufyllin-GG® (containing Dyphylline, Guaifenesin)
* Mintuss® G (containing Guaifenesin, Hydrocodone, Phenylephrine)
* Mucinex® Cold (containing Guaifenesin, Phenylephrine)
* Mucinex® Cough (containing Dextromethorphan, Guaifenesin)
* Mudrane® GG (containing Aminophylline, Ephedrine, Guaifenesin,
Phenobarbital)
* Mytussin® AC (containing Codeine, Guaifenesin)
* Mytussin® DM (containing Dextromethorphan, Guaifenesin)
* Naldecon® DX (containing Dextromethorphan, Guaifenesin)
* Narcof® (containing Guaifenesin, Hydrocodone)
* Nariz® (containing Guaifenesin, Phenylephrine)
* Nazarin® (containing Guaifenesin, Phenylephrine)
* Nortuss® EX (containing Dextromethorphan, Guaifenesin)
* Numonyl® DX (containing Dextromethorphan, Guaifenesin, Phenylephrine)
* Oratuss® (containing Carbetapentane, Guaifenesin)
* Panfil® (containing Dyphylline, Guaifenesin)
* Primatene® (containing Ephedrine, Guaifenesin)
* Prometh with Codeine (containing Codeine, Guaifenesin, Promethazine)
* Q-Tussin® DM (containing Dextromethorphan, Guaifenesin)
* Qual-Tussin® DC (containing Guaifenesin, Hydrocodone, Phenylephrine)
* Quibron® (containing Guaifenesin, Theophylline)
* Robafen® DM (containing Dextromethorphan, Guaifenesin)
* Robitussin® DM (containing Dextromethorphan, Guaifenesin)
* Scot-Tussin® (containing Dextromethorphan, Guaifenesin)
* Siltussin-DM® (containing Dextromethorphan, Guaifenesin)
* Simuc-DM® (containing Dextromethorphan, Guaifenesin)
* Simuc-HD® (containing Guaifenesin, Hydrocodone, Phenylephrine)
* Sine-Off® Cold and Cough (containing Acetaminophen, Dextromethorphan,
Guaifenesin)
* Sitrex® (containing Guaifenesin, Phenylephrine)
* Slo-Phyllin® GG (containing Guaifenesin, Theophylline)
* Sudafed® PE Cold & Cough (containing Acetaminophen, Dextromethorphan,
Guaifenesin, Phenylephrine)
* Theocon® (containing Guaifenesin, Theophylline)
* Theolate® (containing Guaifenesin, Theophylline)
* Theomar G.G.® (containing Guaifenesin, Theophylline)
* Theophyll-GG® (containing Guaifenesin, Theophylline)
* Theospect® (containing Dyphylline, Guaifenesin)
* Theraflu® Flu & Chest Congestion (containing Acetaminophen,
Guaifenesin)
* Triaminic® Chest & Nasal Congestion (containing Guaifenesin,
Phenylephrine)
* Trispec® DMX (containing Dextromethorphan, Guaifenesin)
* Trituss® (containing Dextromethorphan, Guaifenesin, Phenylephrine)
* Tusnel® (containing Brompheniramine, Dextromethorphan, Guaifenesin)
* Tussi Organidin® (containing Codeine, Guaifenesin)
* Tussidin® DM (containing Dextromethorphan, Guaifenesin)
* Tylenol® Chest Congestion (containing Acetaminophen, Guaifenesin)
* Tylenol® Sinus Congestion and Pain Severe (containing Acetaminophen,
Guaifenesin, Phenylephrine)
* Vicks® 44E (containing Dextromethorphan, Guaifenesin)
* Vicotuss® (containing Guaifenesin, Hydrocodone)
* Zotex® (containing Dextromethorphan, Guaifenesin, Phenylephrine)
* Zyrphen® (containing Guaifenesin, Phenylephrine)
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