Fenticol may be available in the countries listed below.
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Losartan potassium salt (a derivative of Losartan) is reported as an ingredient of Anreb in the following countries:
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Class: Oxytocics
ATC Class: G02AD02
VA Class: HS875
Chemical Name: (5Z, 11a, 13E, 15S)-11,15-Dihydroxy-9-oxo-prosta-5,13-dien-1-oic acid
Molecular Formula: C20H32O5
CAS Number: 363-24-6
Brands: Cervidil, Prepidil, Prostin E2
Stimulates uterine smooth muscle and also produces cervical dilation and softening; prostaglandin E2.a 200 213 214
Termination of intrauterine pregnancy during the second trimester (12–20th week of gestation, dated from the first day of the last menstrual period).a e 200
For termination of pregnancy, has been used in conjunction with oxytocin to reduce the dinoprostone dose and number of adverse effects associated with dinoprostone.a e f
Evacuation of uterine contents in cases of missed abortion, intrauterine fetal death up to 28 weeks of gestational age, or nonmetastatic gestational trophoblastic disease (benign hydatidiform mole).a e 200
Treatment to improve cervical inducibility (cervical “ripening”) in pregnant women at or near term with a medical or obstetrical need for labor induction.212 213 216 217 218 219 220 h
Has been used in the management of postpartum hemorrhage†.g
Administer intravaginally as a vaginal suppository (Prostin E2), cervical gel (Prepidil), or vaginal insert (Cervidil).200 212 213
Allow suppository to reach room temperature just prior to administration.200
Remove the foil wrapper and insert the suppository high into the posterior vaginal fornix.200 a Patient should remain supine for 10 minutes following each insertion.200 May require the use of a diaphragm to prevent displacement of the suppository from the paracervical area.a
Allow the gel to reach room temperature just prior to administration; do not use a water bath or other source of external heat (e.g., microwave oven) to facilitate the warming process.212
Consult the manufacturer’s instructions for proper assembly of the syringe and catheter.212
Administer the cervical gel (supplied in a syringe) through a shielded catheter into the cervical canal.212 Select the proper size catheter based on the degree of effacement; if no effacement is present, use the 20-mm catheter; for 50% effacement, use the 10-mm catheter.212
Place patient in a dorsal position and visualize the cervix using a speculum.212 Using sterile technique, introduce the gel via the catheter into the cervical canal, just below the level of the internal os.212 Remove the catheter.212 Patient should remain supine for at least 15–30 minutes to minimize leakage from the cervical canal.212
Keep frozen until use.d
After removal from the protective package (tear at designated mark),d place the vaginal insert transversely in the posterior fornix of the vagina.213 May use a small amount of water-soluble lubricant to assist insertion; excess contact or coating with lubricant may prevent optimal swelling and release of dinoprostone from the insert.213 Patient should remain supine for 2 hours following insertion.213 If patient is ambulatory, ensure that the vaginal insert remains in place.d
Use the knitted polyester retrieval system to aid in drug retrieval at the end of the dosing interval.213 Upon removal of the insert, ensure that the slab is removed.d If the slab is not found in the retrieval system, perform a vaginal examination to remove the slab.d
Dinoprostone vaginal suppositories and any preparation made extemporaneously from dinoprostone vaginal suppositories should not be used at term for cervical “ripening”;200 dinoprostone cervical gel and vaginal insert are used at or near term to improve cervical inducibility.212 213
Dinoprostone vaginal suppositories should not be used for extemporaneous preparation of any other dosage form.200
Vaginal suppositories: 20 mg every 3–5 hours until abortion occurs; adjust the dosing intervals according to abortifacient progress, uterine contractility, and patient tolerance.a 200
Vaginal suppositories: Initial dose of 5 mg, repeated as needed, when used for intrauterine fetal death at >24 weeks’ gestational age.e (See Prescribing Limits.)
Cervical gel: Initially, 0.5 mg (2.5 mL of gel).212 If there is no cervical and/or uterine response to the initial dose, administer another 0.5-mg dose after 6–12 hours.212 220 Clinician should determine the need for additional doses and the dosing intervals.212
Vaginal insert: 1 insert delivering dinoprostone 0.3 mg/hour for 12 hours.213 Remove after 12 hours, at the onset of active labor, or if uterine hyperstimulation develops.213 d
Vaginal suppositories: 20 mg every 2 hours has been used.g
Intravaginal Vaginal suppositories: Use for >2 days not recommended.200
Vaginal suppositories: Initially 5 mg; repeat as needed when used for intrauterine fetal death at >24 weeks, gestational age.e Use of 20-mg dose may result in uterine rupture.e
Cervical gel: Maximum cumulative dose is 1.5 mg (7.5 mL)/24 hours.212 220
Known hypersensitivity to prostaglandins or any ingredient in the formulation.200 212 213
Dinoprostone vaginal suppositories are contraindicated in patients with acute pelvic inflammatory disease and in those with active cardiac, pulmonary, renal, or hepatic disease.200
Dinoprostone cervical gel and vaginal inserts are contraindicated in patients with contraindications to oxytocic agents and when prolonged contractions of the uterus are inappropriate (e.g., previous cesarean section, previous major uterine surgery, history of difficult labor and/or traumatic delivery, marked cephalopelvic disproportion, unfavorable fetal position, ≥6 previous term pregnancies, fetal distress when delivery is not imminent, hyperactive or hypertonic uterus, obstetric emergencies where maternal or fetal risk-to-benefit ratio favors surgery).212 213
Dinoprostone cervical gel and vaginal inserts are contraindicated in patients with placenta previa or unexplained vaginal bleeding during the current pregnancy.212 213
Dinoprostone cervical gel is contraindicated when vaginal delivery is not indicated (e.g., vasa previa, active genital herpes infection).212
The manufacturer of dinoprostone vaginal inserts states that this preparation is contraindicated in patients receiving IV oxytocic therapy.213
Administer by qualified professional personnel in a hospital where intensive care and surgical facilities are immediately available.a 200 212
Dinoprostone does not affect the fetoplacental unit.200 Possibility exists that a previable fetus could exhibit transient signs of life following dinoprostone-induced abortion; dinoprostone is not indicated if the fetus has reached the stage of viability.200 If pregnancy is terminated because of late fetal intrauterine death, confirm fetal death prior to administration of dinoprostone.200
If the pregnancy is not terminated with dinoprostone, complete abortion by another method.200
Confirm pregnancy termination for pregnancy diagnosed as missed abortion.200
Monitor uterine contractions, fetal status (e.g., heart rate), and progression of cervical dilation and effacement of the cervix to avoid complications.220 212 213
Use with caution in patients with ruptured membranes.c d
Carefully select patients; evaluate both maternal and fetal condition before dinoprostone use.212 213 220 (See Contraindications.)
Consider removing dinoprostone vaginal insert if sustained uterine contractions, fetal distress, or other fetal or maternal adverse effects occur.213 Remove the insert if uterine hyperstimulation develops or labor starts.213 Remove the insert before amniotomy.213
Proliferation of long bones reported in neonates receiving long-term therapy with alprostadil (prostaglandin E1).200 a i No evidence that short-term administration of dinoprostone has similar effects on bone.200 a
Caution in patients with cervicitis, infected endocervical lesions, acute vaginitis, compromised (scarred) uterus, asthma or a history of asthma, hypertension or hypotension, seizure disorders, diabetes mellitus, glaucoma, increased IOP, anemia, jaundice, or cardiovascular, renal, or hepatic disease.200 212 213 a b
Transient fever (i.e., temperature elevations >1.1°C) reported.200 When used for termination of pregnancy, may be difficult to distinguish drug-induced temperature elevations from post-abortion endometritis.200
Category C.200 212 213
Safety and efficacy not established in children.200 212 213 Safety and efficacy in adolescents expected to be the same as in adults.213
Use with caution.200 212
Dinoprostone vaginal suppositories are contraindicated in patients with active hepatic disease.200
Use with caution.200 212
Dinoprostone vaginal suppositories are contraindicated in patients with active renal disease.200
Dinoprostone vaginal suppositories: Vomiting, transient fever, diarrhea, nausea, headache, chills, transient DBP decreases of >20 mm Hg.200
Dinoprostone cervical gel or vaginal insert: Uterine hyperstimulation, fetal heart rate abnormality, adverse GI effects, back pain, fever.212 213
Drug | Interaction | Comments |
|---|---|---|
Oxytocic agents (e.g., oxytocin) | May increase activity of other oxytocic agents200 212 213 | Concomitant use not recommended200 212 213 Dinoprostone cervical gel: Allow an inteval of 6–12 hours between administration of the cervical gel and initiation of IV oxytocin212 220 Dinoprostone vaginal insert: Wait ≥30 minutes between removal of dinoprostone vaginal insert and initiation of IV oxytocin213 220 |
Absorbed systemically following vaginal administration as dinoprostone suppositories; a small amount of drug is absorbed directly by the uterus through the cervix or local lymphatic or vascular channels.a
Dinoprostone cervical gel: Peak plasma concentrations achieved in 30–45 minutes.212
Dinoprostone vaginal insert: A controlled-release preparation designed to release 0.3 mg of dinoprostone per hour for 12 hours.213
Dinoprostone vaginal suppositories: Slight uterine contractions begin within 10 minutes (first and second trimester pregnancies).a
Dinoprostone vaginal suppositories: Contractions continue for 2–3 hours (first and second trimester pregnancies).a
Widely distributed in the mother.a
Rapidly metabolized in the maternal lungs, kidneys, spleen, and other tissues, primarily by oxidation of the side chains to at least 9 inactive metabolites.a
Drug and its metabolites excreted principally in urine; small amounts excreted in feces.a
2.5–5 minutes.213
2–8°C.212
-20°C to -10°C.213 Protect from moisture and humidity.213
Do not exceed -20°C.200
Elicits pharmacologic responses usually produced by endogenous prostaglandin E2.200 212 213
Increases the amplitude and frequency of uterine contractions throughout pregnancy; uterine response to the drug increases with the duration of pregnancy.a
Produces local cervical effects including softening, effacement, and dilation.212 213 214
Causes stimulation of the circular smooth muscle of the GI tract, increasing GI motility. a
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.200 212 213
Importance of informing patients of other important precautionary information.200 212 213 (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
|---|---|---|---|---|
Vaginal | Gel | 0.5 mg/3 g | Prepidil | Pfizer |
Insert | 10 mg | Cervidil | Forest | |
Suppositories | 20 mg | Prostin E2 | Pfizer |
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions January 2008. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
† Use is not currently included in the labeling approved by the US Food and Drug Administration.
200. Pharmacia & Upjohn Company. Prostin E2 (dinoprostone vaginal suppository) prescribing information (dated 1999 Aug). In: Physician’s desk reference. 55th ed. Montvale, NJ: Medical Economics Company Inc; 2001:2638-9.
201. Rayburn W, Gosen R, Ramadei C et al. Outpatient cervical ripening with prostaglandin E2 gel in uncomplicated postdate pregnancies. Am J Obstet Gynecol. 1988; 158:1417-23. [IDIS 310426] [PubMed 3289398]
202. Nager CW, Key TC, Moore TR. Cervical ripening and labor outcome with preinduction intracervical prostaglandin E2 (Prepidil) gel. J Perinatol. 1987; 7:189-93. [PubMed 3504454]
203. Trofatter KF Jr, Bowers D, Gall SA et al. Preinduction cervical ripening with prostaglandin E2 (Prepidil) gel. Am J Obstet Gynecol. 1985; 153:268-71. [IDIS 207501] [PubMed 3901764]
204. Neilson DR Jr, Prins RP, Bolton RN et al. A comparison of prostaglandin E2 gel and prostaglandin F2α gel for preinduction cervical ripening. Am J Obstet Gynecol. 1983; 146:526-32. [IDIS 172356] [PubMed 6344644]
205. Lorenz RP, Botti JJ, Chez RA et al. Variations of biologic activity of low-dose prostaglandin E2 on cervical ripening. Obstet Gynecol. 1984; 64:123-7. [IDIS 187151] [PubMed 6377145]
206. Prins RP, Bolton RN, Mark C III et al. Cervical ripening with intravaginal prostaglandin E2 gel. Obstet Gynecol. 1983; 61:459-62. [IDIS 168236] [PubMed 6572335]
207. Ulmsten U, Wingerup L, Andersson KE. Comparison of prostaglandin E2 and intravenous oxytocin for induction of labor. Obstet Gynecol. 1979; 54:581-4. [IDIS 107185] [PubMed 503385]
208. Dingfelder JR, Brenner WE, Hendricks CH et al. Reduction of cervical resistance by prostaglandin suppositories prior to dilatation for induced abortion. Am J Obstet Gynecol. 1975; 122:25-30. [PubMed 1130444]
209. Jagani N, Schulman H, Fleischer A et al. Role of prostaglandin-induced cervical changes in labor induction. Obstet Gynecol. 1984; 63:225-9. [IDIS 181001] [PubMed 6582419]
210. Buchanan D, Macer J, Yonekura ML. Cervical ripening with prostaglandin E2 vaginal suppositories. Obstet Gynecol. 1984; 63:659-63. [IDIS 184594] [PubMed 6585733]
211. Lagrew DC, Freeman RK. Management of postdate pregnancy. Am J Obstet Gynecol. 1986; 154:8-13. [PubMed 3946506]
212. Pharmacia & Upjohn Company. Prepidil Gel (dinoprostone cervical gel) prescribing information (dated 1999 Apr). In: Physician’s desk reference. 55th ed. Montvale, NJ: Medical Economics Company Inc; 2001:2637-8.
213. Forest Pharmaceuticals. Cervidil (dinoprostone vaginal insert) prescribing information (dated 2000 Feb). In: Physician’s desk reference. 55th ed. Montvale, NJ: Medical Economics Company Inc; 2001:1261-3.
214. Bryman I, Norstrom A, Lindblom B. Has cervical smooth muscle any physiological role in the human? Acta Physiol Hung. 1985; 65:327-30.
215. MacLennan AH, Katz M, Creasy R. The morphologic characteristics of cervical ripening induced by the hormones relaxin and prostaglandin F2 alpha in a rabbit model. Am J Obstet Gynecol. 1985; 152(6 pt 1):691-6. [PubMed 3861093]
216. Sadaty A, Pagano M, Greer C et al. A randomized trial of vaginal prostaglandin E(2) gel and dinoprostone vaginal insert for induction of labor at term. Prim Care Update Ob Gyns. 1998; 5:183. [PubMed 10838343]
217. Warke HS, Saraogi RM, Sanjwalla SM. Prostaglandin E2 gel In ripening of cervix in induction of labour. J Postgrad Med. 1999; 45:105-9. [PubMed 10734347]
218. Wieland D, Friedman F Jr. Comparing two dinoprostone agents for preinduction cervical ripening at term: a randomized trial. J Reprod Med. 1999; 44:724-8. [IDIS 435924] [PubMed 10483544]
219. McKenna DS, Costa SW, Samuels P. Prostaglandin E2 cervical ripening without subsequent induction of labor. Obstet Gynecol. 1999; 94:11-4. [IDIS 430673] [PubMed 10389710]
220. American College of Obstetricians and Gynecologists (ACOG) Committee on Practice Bulletins. Induction of labor. Practice Bulletin No. 10. Washington, DC: American College of Obstetricians and Gynecologists; 1999 Nov.
a. AHFS Drug Information 2007. McEvoy GK, ed. Dinoprostone. Bethesda, MD: American Society of Health-System Pharmacists; 2007: 3267-9.
b. Pharmacia and UpJohn. Prostin E2 (dinoprostone) vaginal suppository prescribing information. New York, NY; 2006 Apr..
c. Pharmacia and UpJohn . Prepidil (dinoprostone) cervical gel prescribing information. New York, NY; 2006 Nov.
d. Forest Pharmaceuticals, Inc. Cervidil (dinoprostone) vaginal insert prescribing information. St Louis, MO; 2006 May.
e. Stubblefield PG, Carr-Ellis S, Borgatta L. Methods for induced abortion. Obstet Gynecol. 2004; 104:174-85. [PubMed 15229018]
f. Ramsey PS, Savage K, Lincoln T, Owen J. Vaginal misoprostol versus concentrated oxytocin and vaginal PGE2 for second-trimester labor induction. Obstet Gynecol. 2004; 104:138-45. [PubMed 15229013]
g. American College of Obstetricians and Gynecologists (ACOG) Committee Practice Bulletin. Postpartum hemorrhage. Practice Bulletin No. 76. Washington, DC: American College of Obstetricians and Gynecologists; 2006 Oct.
h. Briggs GG, Wan SR. Drug therapy during labor and delivery, part 2. Am J Health-Syst Pharm. 2006; 63:1131-9. [PubMed 16754739]
i. Pharmacia. Prostin VR Pediatric (alprostadil) injection prescribing information. Kalamazoo, MI; 2002 Aug.
Generic Name: carbetapentane and pseudoephedrine (kar BAY ta PEN tane and SOO doe ee FED rin)
Brand Names: Allres Pd, Carb Pseudo-Tan, Corzall, Pseudacarb, Re-Tann, Respi-TANN, Respi-Tann Pd
Pseudoephedrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).
Carbetapentane is a cough suppressant. It affects the signals in the brain that trigger cough reflex.
The combination of carbetapentane and pseudoephedrine is used to treat cough and nasal and sinus congestion caused by the common cold, flu, or bronchitis.
Carbetapentane and pseudoephedrine may also be used for purposes not listed in this medication guide.
To make sure you can safely take carbetapentane and pseudoephedrine, tell your doctor if you have any of these other conditions:
heart disease or high blood pressure;
a seizure disorder;
glaucoma;
an enlarged prostate or problems with urination;
diabetes; or
a thyroid disorder.
Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.
Measure liquid medicine with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.
The chewable tablet must be chewed before you swallow it.
If you need surgery, tell the surgeon ahead of time if you have taken a cough or cold medicine within the past few days.
Since cough or cold medicine is taken when needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.
Avoid taking this medication if you also take diet pills, caffeine pills, or other stimulants (such as ADHD medications). Taking a stimulant together with a decongestant can increase your risk of unpleasant side effects.
fast, pounding, or uneven heartbeat;
severe dizziness, anxiety, restless feeling, or nervousness;
confusion, hallucinations;
slow, shallow breathing;
easy bruising or bleeding, unusual weakness, fever, chills, body aches, flu symptoms; or
dangerously high blood pressure (severe headache, blurred vision, ringing in your ears, anxiety, confusion, chest pain, trouble breathing, uneven heart rate, seizure).
Less serious side effects may include:
loss of appetite, upset stomach;
warmth, redness, or tingling under your skin;
feeling excited or restless;
sleep problems (insomnia); or
mild skin rash or itching.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Tell your doctor about all other medicines you use, especially:
celecoxib (Celebrex);
cinacalcet (Sensipar);
darifenacin (Enablex);
imatinib (Gleevec);
quinidine (Quin-G);
ranolazine (Ranexa)
ritonavir (Norvir, Kaletra);
sibutramine (Meridia);
terbinafine (Lamisil);
medicines to treat high blood pressure;
an antidepressant such as amitriptyline (Elavil, Vanatrip), bupropion (Wellbutrin, Zyban), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), imipramine (Janimine, Tofranil), paroxetine (Paxil), sertraline (Zoloft), and others; or
a beta-blocker such as atenolol (Tenormin, Tenoretic), carvedilol (Coreg), labetalol (Normodyne, Trandate), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal, InnoPran), sotalol (Betapace), and others.
This list is not complete and other drugs may interact with carbetapentane and pseudoephedrine. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.
See also: Re-Tann side effects (in more detail)
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In the US, Afinitor (everolimus systemic) is a member of the following drug classes: mTOR inhibitors, selective immunosuppressants and is used to treat Brain Tumor, Pancreatic Cancer and Renal Cell Carcinoma.
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In some countries, this medicine may only be approved for veterinary use.
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