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Cytotec
Overview
What is Cytotec?
Cytotec oral tablets contain either 100 mcg or 200 mcg of
misoprostol, a synthetic prostaglandin E analog.
Misoprostol contains approximately equal amounts of the two diastereomers
presented below with their enantiomers indicated by (±):
Misoprostol is a water-soluble, viscous liquid.
Inactive ingredients of tablets are hydrogenated castor oil, hypromellose,
microcrystalline cellulose, and sodium starch glycolate.
What does Cytotec look like?
What are the available doses of Cytotec?
Sorry No records found.
What should I talk to my health care provider before I take Cytotec?
Sorry No records found
How should I use Cytotec?
Cytotec (misoprostol) is indicated for reducing the risk of NSAID (nonsteroidal
anti-inflammatory drugs, including aspirin)–induced gastric ulcers in patients
at high risk of complications from gastric ulcer, e.g., the elderly and patients
with concomitant debilitating disease, as well as patients at high risk of
developing gastric ulceration, such as patients with a history of ulcer. Cytotec
has not been shown to reduce the risk of duodenal ulcers in patients taking
NSAIDs. Cytotec should be taken for the duration of NSAID therapy. Cytotec has
been shown to reduce the risk of gastric ulcers in controlled studies of 3
months' duration. It had no effect, compared to placebo, on gastrointestinal
pain or discomfort associated with NSAID use.
The recommended adult oral dose of Cytotec for reducing the risk
of NSAID-induced gastric ulcers is 200 mcg four times daily with food. If this
dose cannot be tolerated, a dose of 100 mcg can be used. (See .) Cytotec should be taken for the duration of NSAID
therapy as prescribed by the physician. Cytotec should be taken with a meal, and
the last dose of the day should be at bedtime.
Adjustment of the dosing schedule in renally impaired patients is
not routinely needed, but dosage can be reduced if the 200-mcg dose is not
tolerated. (See .)
What interacts with Cytotec?
See boxed
Cytotec should not be taken by pregnant women to reduce the risk of ulcers induced by nonsteroidal anti-inflammatory drugs (NSAIDs).
Cytotec should not be taken by anyone with a history of allergy to prostaglandins.
What are the warnings of Cytotec?
Array
What are the precautions of Cytotec?
Caution should be employed when administering Cytotec
(misoprostol) to patients with pre-existing cardiovascular disease.
Women of childbearing potential using Cytotec to decrease the
risk of NSAID-induced ulcers should be told that they must not be pregnant when
Cytotec therapy is initiated, and that they must use an effective contraception
method while taking Cytotec.
See boxed
Cytotec is intended for administration along with nonsteroidal
anti-inflammatory drugs (NSAIDs), including aspirin, to decrease the chance of
developing an NSAID-induced gastric ulcer.
Cytotec should be taken only according to the directions given by a
physician.
If the patient has questions about or problems with Cytotec, the physician
should be contacted promptly.
THE PATIENT SHOULD NOT GIVE CYTOTEC TO ANYONE ELSE.
The Cytotec package the patient receives from the pharmacist will include a
leaflet containing patient information. The patient should read the leaflet
before taking Cytotec and each time the prescription is renewed because the
leaflet may have been revised.
Keep Cytotec out of the reach of children.
SPECIAL NOTE FOR WOMEN: Cytotec may cause abortion
(sometimes incomplete), premature labor, or birth defects if given to pregnant
women.
Cytotec is available only as a unit-of-use package that includes a leaflet
containing patient information. See at the end of this
labeling.
See . Cytotec has not been shown to interfere with the
beneficial effects of aspirin on signs and symptoms of rheumatoid arthritis.
Cytotec does not exert clinically significant effects on the absorption, blood
levels, and antiplatelet effects of therapeutic doses of aspirin. Cytotec has no
clinically significant effect on the kinetics of diclofenac or ibuprofen.
A reversible increase in the number of normal surface gastric
epithelial cells occurred in the dog, rat, and mouse. No such increase has been
observed in humans administered Cytotec for up to 1 year.
An apparent response of the female mouse to Cytotec in long-term studies at
100 to 1000 times the human dose was hyperostosis, mainly of the medulla of
sternebrae. Hyperostosis did not occur in long-term studies in the dog and rat
and has not been seen in humans treated with Cytotec.
There was no evidence of an effect of Cytotec on tumor occurrence
or incidence in rats receiving daily doses up to 150 times the human dose for 24
months. Similarly, there was no effect of Cytotec on tumor occurrence or
incidence in mice receiving daily doses up to 1000 times the human dose for 21
months. The mutagenic potential of Cytotec was tested in several assays, all of which were negative.
Misoprostol, when administered to breeding male and female rats at doses 6.25
times to 625 times the maximum recommended human therapeutic dose, produced
dose-related pre- and post-implantation losses and a significant decrease in the
number of live pups born at the highest dose. These findings suggest the
possibility of a general adverse effect on fertility in males and females.
See boxed Congenital anomalies sometimes
associated with fetal death have been reported subsequent to the unsuccessful
use of misoprostol as an abortifacient, but the drug's teratogenic mechanism has
not been demonstrated. Several reports in the literature associate the use of
misoprostol during the first trimester of pregnancy with skull defects, cranial
nerve palsies, facial malformations, and limb defects.
Cytotec is not fetotoxic or teratogenic in rats and rabbits at doses 625 and
63 times the human dose, respectively.
See boxed . Cytotec may endanger pregnancy (may
cause abortion) and thereby cause harm to the fetus when administered to a
pregnant woman. Cytotec may produce uterine contractions, uterine bleeding, and
expulsion of the products of conception. Abortions caused by Cytotec may be
incomplete. If a woman is or becomes pregnant while taking this drug to reduce
the risk of NSAID-induced ulcers, the drug should be discontinued and the
patient apprised of the potential hazard to the fetus.
Cytotec can induce or augment uterine contractions. Vaginal
administration of Cytotec, outside of its approved indication, has been used as
a cervical ripening agent, for the induction of labor and for treatment of
serious postpartum hemorrhage in the presence of uterine atony. A major adverse
effect of the obstetrical use of Cytotec is the hyperstimulation of the uterus
which may progress to uterine tetany with marked impairment of uteroplacental
blood flow, uterine rupture (requiring surgical repair, hysterectomy, and/or
salpingo-oophorectomy), or amniotic fluid embolism. Pelvic pain, retained
placenta, severe genital bleeding, shock, fetal bradycardia, and fetal and
maternal death have been reported.
There may be an increased risk of uterine tachysystole, uterine rupture,
meconium passage, meconium staining of amniotic fluid, and Cesarean delivery due
to uterine hyperstimulation with the use of higher doses of Cytotec, including
the manufactured 100 mcg tablet. The risk of uterine rupture increases with
advancing gestational ages and with prior uterine surgery, including Cesarean
delivery. Grand multiparity also appears to be a risk factor for uterine
rupture.
The effect of Cytotec on later growth, development, and functional maturation
of the child when Cytotec is used for cervical ripening or induction of labor
has not been established. Information on Cytotec's effect on the need for
forceps delivery or other intervention is unknown.
Misoprostol is rapidly metabolized in the mother to misoprostol
acid, which is biologically active and is excreted in breast milk. There are no
published reports of adverse effects of misoprostol in breast-feeding infants of
mothers taking misoprostol. Caution should be exercised when misoprostol is
administered to a nursing woman.
Safety and effectiveness of Cytotec in pediatric patients have
not been established.
What are the side effects of Cytotec?
The following have been reported as adverse events in subjects
receiving Cytotec:
In subjects receiving Cytotec 400 or 800 mcg daily in clinical
trials, the most frequent gastrointestinal adverse events were diarrhea and
abdominal pain. The incidence of diarrhea at 800 mcg in controlled trials in
patients on NSAIDs ranged from 14–40% and in all studies (over 5,000 patients)
averaged 13%. Abdominal pain occurred in 13–20% of patients in NSAID trials and
about 7% in all studies, but there was no consistent difference from
placebo.
Diarrhea was dose related and usually developed early in the course of
therapy (after 13 days), usually was self-limiting (often resolving after 8
days), but sometimes required discontinuation of Cytotec (2% of the patients).
Rare instances of profound diarrhea leading to severe dehydration have been
reported. Patients with an underlying condition such as inflammatory bowel
disease, or those in whom dehydration, were it to occur, would be dangerous,
should be monitored carefully if Cytotec is prescribed. The incidence of
diarrhea can be minimized by administering after meals and at bedtime, and by
avoiding coadministration of Cytotec with magnesium-containing antacids.
Women who received Cytotec during clinical trials reported the
following gynecological disorders: spotting (0.7%), cramps (0.6%),
hypermenorrhea (0.5%), menstrual disorder (0.3%) and dysmenorrhea (0.1%).
Postmenopausal vaginal bleeding may be related to Cytotec administration. If it
occurs, diagnostic workup should be undertaken to rule out gynecological
pathology. (See boxed )
There were no significant differences in the safety profile of
Cytotec in approximately 500 ulcer patients who were 65 years of age or older
compared with younger patients.
Additional adverse events which were reported are categorized as
follows:
In clinical trials, the following adverse reactions were reported
by more than 1% of the subjects receiving Cytotec and may be causally related to
the drug: nausea (3.2%), flatulence (2.9%), headache (2.4%), dyspepsia (2.0%),
vomiting (1.3%), and constipation (1.1%). However, there were no significant
differences between the incidences of these events for Cytotec and
placebo.
The following adverse events were infrequently reported. Causal
relationships between Cytotec and these events have not been established but
cannot be excluded:
Body as a whole:
Skin:
Special senses:
Respiratory:
Cardiovascular:
Gastrointestinal:
Hypersensitivity:
Metabolic:
Genitourinary:
Nervous system/Psychiatric:
Musculoskeletal:
Blood/Coagulation:
What should I look out for while using Cytotec?
See boxed
Cytotec should not be taken by pregnant women to reduce the
risk of ulcers induced by nonsteroidal anti-inflammatory drugs (NSAIDs).
Cytotec should not be taken by anyone with a history of allergy to
prostaglandins.
See boxed
What might happen if I take too much Cytotec?
The toxic dose of Cytotec in humans has not been determined.
Cumulative total daily doses of 1600 mcg have been tolerated, with only symptoms
of gastrointestinal discomfort being reported. In animals, the acute toxic
effects are diarrhea, gastrointestinal lesions, focal cardiac necrosis, hepatic
necrosis, renal tubular necrosis, testicular atrophy, respiratory difficulties,
and depression of the central nervous system. Clinical signs that may indicate
an overdose are sedation, tremor, convulsions, dyspnea, abdominal pain,
diarrhea, fever, palpitations, hypotension, or bradycardia. Symptoms should be
treated with supportive therapy.
It is not known if misoprostol acid is dialyzable. However, because
misoprostol is metabolized like a fatty acid, it is unlikely that dialysis would
be appropriate treatment for overdosage.
How should I store and handle Cytotec?
Store at 20°-25°C (68°-77°F) (see USP Controlled Room Temperature). PROTECT FROM LIGHT. KEEP TIGHTLY CLOSED. Sarafem is a registered trademark of Eli Lilly and Company. Cytotec 100-mcg tablets are white, round, with SEARLE debossed on one side and 1451 on the other side; supplied as:NDC NumberSizeStore at or below 25°C (77°F), in a dry area.Cytotec 100-mcg tablets are white, round, with SEARLE debossed on one side and 1451 on the other side; supplied as:NDC NumberSizeStore at or below 25°C (77°F), in a dry area.Cytotec 100-mcg tablets are white, round, with SEARLE debossed on one side and 1451 on the other side; supplied as:NDC NumberSizeStore at or below 25°C (77°F), in a dry area.Cytotec 100-mcg tablets are white, round, with SEARLE debossed on one side and 1451 on the other side; supplied as:NDC NumberSizeStore at or below 25°C (77°F), in a dry area.
Clinical Information
Chemical Structure
No Image foundClinical Pharmacology
Misoprostol is extensively absorbed, and undergoes rapid
de-esterification to its free acid, which is responsible for its clinical
activity and, unlike the parent compound, is detectable in plasma. The alpha
side chain undergoes beta oxidation and the beta side chain undergoes omega
oxidation followed by reduction of the ketone to give prostaglandin F
analogs.
In normal volunteers, Cytotec (misoprostol) is rapidly absorbed after oral
administration with a T of misoprostol acid of 12 ± 3
minutes and a terminal half-life of 20–40 minutes.
There is high variability of plasma levels of misoprostol acid between and
within studies but mean values after single doses show a linear relationship
with dose over the range of 200–400 mcg. No accumulation of misoprostol acid was
noted in multiple dose studies; plasma steady state was achieved within two
days.
Maximum plasma concentrations of misoprostol acid are diminished when the
dose is taken with food and total availability of misoprostol acid is reduced by
use of concomitant antacid. Clinical trials were conducted with concomitant
antacid, however, so this effect does not appear to be clinically important.
After oral administration of radiolabeled misoprostol, about 80% of detected
radioactivity appears in urine. Pharmacokinetic studies in patients with varying
degrees of renal impairment showed an approximate doubling of T, C, and AUC compared to normals,
but no clear correlation between the degree of impairment and AUC. In subjects
over 64 years of age, the AUC for misoprostol acid is increased. No routine
dosage adjustment is recommended in older patients or patients with renal
impairment, but dosage may need to be reduced if the usual dose is not
tolerated.
Drug interaction studies between misoprostol and several nonsteroidal
anti-inflammatory drugs showed no effect on the kinetics of ibuprofen or
diclofenac, and a 20% decrease in aspirin AUC, not thought to be clinically
significant.
Pharmacokinetic studies also showed a lack of drug interaction with
antipyrine and propranolol when these drugs were given with misoprostol.
Misoprostol given for 1 week had no effect on the steady state pharmacokinetics
of diazepam when the two drugs were administered 2 hours apart.
The serum protein binding of misoprostol acid is less than 90% and is
concentration-independent in the therapeutic range.
After a single oral dose of misoprostol to nursing mothers, misoprostol acid
was excreted in breast milk. The maximum concentration of misoprostol acid in
expressed breast milk was achieved within 1 hour after dosing and was 7.6 pg/ml
(CV 37%) and 20.9 pg/ml (CV 62%) after single 200 µg and 600 µg misoprostol
administration, respectively. The misoprostol acid concentrations in breast milk
declined to less than 1 pg/ml at 5 hours post-dose.
Misoprostol has both antisecretory (inhibiting gastric acid
secretion) and (in animals) mucosal protective properties. NSAIDs inhibit
prostaglandin synthesis, and a deficiency of prostaglandins within the gastric
mucosa may lead to diminishing bicarbonate and mucus secretion and may
contribute to the mucosal damage caused by these agents. Misoprostol can
increase bicarbonate and mucus production, but in man this has been shown at
doses 200 mcg and above that are also antisecretory. It is therefore not
possible to tell whether the ability of misoprostol to reduce the risk of
gastric ulcer is the result of its antisecretory effect, its mucosal protective
effect, or both.
In vitro
Misoprostol produces a moderate decrease in pepsin concentration during basal
conditions, but not during histamine stimulation. It has no significant effect
on fasting or postprandial gastrin nor on intrinsic factor output.
Misoprostol, over the range of 50–200 mcg, inhibits basal and
nocturnal gastric acid secretion, and acid secretion in response to a variety of
stimuli, including meals, histamine, pentagastrin, and coffee. Activity is
apparent 30 minutes after oral administration and persists for at least 3 hours.
In general, the effects of 50 mcg were modest and shorter lived, and only the
200-mcg dose had substantial effects on nocturnal secretion or on histamine and
meal-stimulated secretion.
Cytotec has been shown to produce uterine contractions that may
endanger pregnancy. (See boxed )
Cytotec does not produce clinically significant effects on serum
levels of prolactin, gonadotropins, thyroid-stimulating hormone, growth hormone,
thyroxine, cortisol, gastrointestinal hormones (somatostatin, gastrin,
vasoactive intestinal polypeptide, and motilin), creatinine, or uric acid.
Gastric emptying, immunologic competence, platelet aggregation, pulmonary
function, or the cardiovascular system are not modified by recommended doses of
Cytotec.
In a series of small short-term (about 1 week) placebo-controlled
studies in healthy human volunteers, doses of misoprostol were evaluated for
their ability to reduce the risk of NSAID-induced mucosal injury. Studies of 200
mcg q.i.d. of misoprostol with tolmetin and naproxen, and of 100 and 200 mcg
q.i.d. with ibuprofen, all showed reduction of the rate of significant
endoscopic injury from about 70–75% on placebo to 10–30% on misoprostol. Doses
of 25–200 mcg q.i.d. reduced aspirin-induced mucosal injury and bleeding.
Two 12-week, randomized, double-blind trials in osteoarthritic
patients who had gastrointestinal symptoms but no ulcer on endoscopy while
taking an NSAID compared the ability of 200 mcg of Cytotec, 100 mcg of Cytotec,
and placebo to reduce the risk of gastric ulcer (GU) formation. Patients were
approximately equally divided between ibuprofen, piroxicam, and naproxen, and
continued this treatment throughout the 12 weeks. The 200-mcg dose caused a
marked, statistically significant reduction in gastric ulcers in both studies.
The lower dose was somewhat less effective, with a significant result in only
one of the studies.
In these trials there were no significant differences between Cytotec and
placebo in relief of day or night abdominal pain. No effect of Cytotec in
reducing the risk of duodenal ulcers was demonstrated, but relatively few
duodenal lesions were seen.
In another clinical trial, 239 patients receiving aspirin 650–1300 mg q.i.d.
for rheumatoid arthritis who had endoscopic evidence of duodenal and/or gastric
inflammation were randomized to misoprostol 200 mcg q.i.d. or placebo for 8
weeks while continuing to receive aspirin. The study evaluated the possible
interference of Cytotec on the efficacy of aspirin in these patients with
rheumatoid arthritis by analyzing joint tenderness, joint swelling, physician's
clinical assessment, patient's assessment, change in ARA classification, change
in handgrip strength, change in duration of morning stiffness, patient's
assessment of pain at rest, movement, interference with daily activity, and ESR.
Cytotec did not interfere with the efficacy of aspirin in these patients with
rheumatoid arthritis.
Non-Clinical Toxicology
See boxedCytotec should not be taken by pregnant women to reduce the risk of ulcers induced by nonsteroidal anti-inflammatory drugs (NSAIDs).
Cytotec should not be taken by anyone with a history of allergy to prostaglandins.
See boxed
Caution should be employed when administering Cytotec (misoprostol) to patients with pre-existing cardiovascular disease.
Women of childbearing potential using Cytotec to decrease the risk of NSAID-induced ulcers should be told that they must not be pregnant when Cytotec therapy is initiated, and that they must use an effective contraception method while taking Cytotec.
See boxed
Cytotec is intended for administration along with nonsteroidal anti-inflammatory drugs (NSAIDs), including aspirin, to decrease the chance of developing an NSAID-induced gastric ulcer.
Cytotec should be taken only according to the directions given by a physician.
If the patient has questions about or problems with Cytotec, the physician should be contacted promptly.
THE PATIENT SHOULD NOT GIVE CYTOTEC TO ANYONE ELSE.
The Cytotec package the patient receives from the pharmacist will include a leaflet containing patient information. The patient should read the leaflet before taking Cytotec and each time the prescription is renewed because the leaflet may have been revised.
Keep Cytotec out of the reach of children.
SPECIAL NOTE FOR WOMEN: Cytotec may cause abortion (sometimes incomplete), premature labor, or birth defects if given to pregnant women.
Cytotec is available only as a unit-of-use package that includes a leaflet containing patient information. See at the end of this labeling.
See . Cytotec has not been shown to interfere with the beneficial effects of aspirin on signs and symptoms of rheumatoid arthritis. Cytotec does not exert clinically significant effects on the absorption, blood levels, and antiplatelet effects of therapeutic doses of aspirin. Cytotec has no clinically significant effect on the kinetics of diclofenac or ibuprofen.
A reversible increase in the number of normal surface gastric epithelial cells occurred in the dog, rat, and mouse. No such increase has been observed in humans administered Cytotec for up to 1 year.
An apparent response of the female mouse to Cytotec in long-term studies at 100 to 1000 times the human dose was hyperostosis, mainly of the medulla of sternebrae. Hyperostosis did not occur in long-term studies in the dog and rat and has not been seen in humans treated with Cytotec.
There was no evidence of an effect of Cytotec on tumor occurrence or incidence in rats receiving daily doses up to 150 times the human dose for 24 months. Similarly, there was no effect of Cytotec on tumor occurrence or incidence in mice receiving daily doses up to 1000 times the human dose for 21 months. The mutagenic potential of Cytotec was tested in several assays, all of which were negative.
Misoprostol, when administered to breeding male and female rats at doses 6.25 times to 625 times the maximum recommended human therapeutic dose, produced dose-related pre- and post-implantation losses and a significant decrease in the number of live pups born at the highest dose. These findings suggest the possibility of a general adverse effect on fertility in males and females.
See boxed Congenital anomalies sometimes associated with fetal death have been reported subsequent to the unsuccessful use of misoprostol as an abortifacient, but the drug's teratogenic mechanism has not been demonstrated. Several reports in the literature associate the use of misoprostol during the first trimester of pregnancy with skull defects, cranial nerve palsies, facial malformations, and limb defects.
Cytotec is not fetotoxic or teratogenic in rats and rabbits at doses 625 and 63 times the human dose, respectively.
See boxed . Cytotec may endanger pregnancy (may cause abortion) and thereby cause harm to the fetus when administered to a pregnant woman. Cytotec may produce uterine contractions, uterine bleeding, and expulsion of the products of conception. Abortions caused by Cytotec may be incomplete. If a woman is or becomes pregnant while taking this drug to reduce the risk of NSAID-induced ulcers, the drug should be discontinued and the patient apprised of the potential hazard to the fetus.
Cytotec can induce or augment uterine contractions. Vaginal administration of Cytotec, outside of its approved indication, has been used as a cervical ripening agent, for the induction of labor and for treatment of serious postpartum hemorrhage in the presence of uterine atony. A major adverse effect of the obstetrical use of Cytotec is the hyperstimulation of the uterus which may progress to uterine tetany with marked impairment of uteroplacental blood flow, uterine rupture (requiring surgical repair, hysterectomy, and/or salpingo-oophorectomy), or amniotic fluid embolism. Pelvic pain, retained placenta, severe genital bleeding, shock, fetal bradycardia, and fetal and maternal death have been reported.
There may be an increased risk of uterine tachysystole, uterine rupture, meconium passage, meconium staining of amniotic fluid, and Cesarean delivery due to uterine hyperstimulation with the use of higher doses of Cytotec, including the manufactured 100 mcg tablet. The risk of uterine rupture increases with advancing gestational ages and with prior uterine surgery, including Cesarean delivery. Grand multiparity also appears to be a risk factor for uterine rupture.
The effect of Cytotec on later growth, development, and functional maturation of the child when Cytotec is used for cervical ripening or induction of labor has not been established. Information on Cytotec's effect on the need for forceps delivery or other intervention is unknown.
Misoprostol is rapidly metabolized in the mother to misoprostol acid, which is biologically active and is excreted in breast milk. There are no published reports of adverse effects of misoprostol in breast-feeding infants of mothers taking misoprostol. Caution should be exercised when misoprostol is administered to a nursing woman.
Safety and effectiveness of Cytotec in pediatric patients have not been established.
The following have been reported as adverse events in subjects receiving Cytotec:
In subjects receiving Cytotec 400 or 800 mcg daily in clinical trials, the most frequent gastrointestinal adverse events were diarrhea and abdominal pain. The incidence of diarrhea at 800 mcg in controlled trials in patients on NSAIDs ranged from 14–40% and in all studies (over 5,000 patients) averaged 13%. Abdominal pain occurred in 13–20% of patients in NSAID trials and about 7% in all studies, but there was no consistent difference from placebo.
Diarrhea was dose related and usually developed early in the course of therapy (after 13 days), usually was self-limiting (often resolving after 8 days), but sometimes required discontinuation of Cytotec (2% of the patients). Rare instances of profound diarrhea leading to severe dehydration have been reported. Patients with an underlying condition such as inflammatory bowel disease, or those in whom dehydration, were it to occur, would be dangerous, should be monitored carefully if Cytotec is prescribed. The incidence of diarrhea can be minimized by administering after meals and at bedtime, and by avoiding coadministration of Cytotec with magnesium-containing antacids.
Women who received Cytotec during clinical trials reported the following gynecological disorders: spotting (0.7%), cramps (0.6%), hypermenorrhea (0.5%), menstrual disorder (0.3%) and dysmenorrhea (0.1%). Postmenopausal vaginal bleeding may be related to Cytotec administration. If it occurs, diagnostic workup should be undertaken to rule out gynecological pathology. (See boxed )
There were no significant differences in the safety profile of Cytotec in approximately 500 ulcer patients who were 65 years of age or older compared with younger patients.
Additional adverse events which were reported are categorized as follows:
In clinical trials, the following adverse reactions were reported by more than 1% of the subjects receiving Cytotec and may be causally related to the drug: nausea (3.2%), flatulence (2.9%), headache (2.4%), dyspepsia (2.0%), vomiting (1.3%), and constipation (1.1%). However, there were no significant differences between the incidences of these events for Cytotec and placebo.
The following adverse events were infrequently reported. Causal relationships between Cytotec and these events have not been established but cannot be excluded:
Body as a whole:
Skin:
Special senses:
Respiratory:
Cardiovascular:
Gastrointestinal:
Hypersensitivity:
Metabolic:
Genitourinary:
Nervous system/Psychiatric:
Musculoskeletal:
Blood/Coagulation:
Reference
This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"
While we update our database periodically, we cannot guarantee it is always updated to the latest version.
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