Vendrex may be available in the countries listed below.
Diclofenac sodium salt (a derivative of Diclofenac) is reported as an ingredient of Vendrex in the following countries:
International Drug Name Search
Cubicin is a brand name of daptomycin, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Cubicin available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cubicin. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Cordarone is a brand name of amiodarone, approved by the FDA in the following formulation(s):
Yes. The following products are equivalent to Cordarone:
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cordarone. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
There are no current U.S. patents associated with Cordarone.
Ran-Lansoprazole may be available in the countries listed below.
Lansoprazole is reported as an ingredient of Ran-Lansoprazole in the following countries:
International Drug Name Search
Piperazin may be available in the countries listed below.
Piperazine hexahydrate (a derivative of Piperazine) is reported as an ingredient of Piperazin in the following countries:
International Drug Name Search
Ramipril/HCT Hexal may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Ramipril/HCT Hexal in the following countries:
Ramipril is reported as an ingredient of Ramipril/HCT Hexal in the following countries:
International Drug Name Search
Loxiflam may be available in the countries listed below.
Meloxicam is reported as an ingredient of Loxiflam in the following countries:
International Drug Name Search
See also: Generic Coreg CR
Coreg is a brand name of carvedilol, approved by the FDA in the following formulation(s):
A generic version of Coreg has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Coreg and have been approved by the FDA:
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Coreg. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
See also: Generic Cordran
Cordran SP is a brand name of flurandrenolide topical, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Cordran SP available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cordran SP. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
There are no current U.S. patents associated with Cordran SP.
Treating acid indigestion, heartburn, and sour stomach. It may also be used for other conditions as determined by your doctor.
Magaldrate Suspension is an antacid. It works by neutralizing stomach acid and increasing the pH of the stomach.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Magaldrate Suspension. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Magaldrate Suspension. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Magaldrate Suspension may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Magaldrate Suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Magaldrate Suspension.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Constipation; diarrhea; intestinal pain.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry stools; loss of appetite; muscle weakness; nausea; slow reflexes; vomiting; vomit that looks like coffee grounds.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Magaldrate side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.
Store Magaldrate Suspension at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Magaldrate Suspension out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Magaldrate Suspension. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Cytoxan is a brand name of cyclophosphamide, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Cytoxan available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cytoxan. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
There are no current U.S. patents associated with Cytoxan.
Metrosil may be available in the countries listed below.
Metronidazole is reported as an ingredient of Metrosil in the following countries:
International Drug Name Search
Tindamax is a brand name of tinidazole, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Tindamax available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Tindamax. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
There are no current U.S. patents associated with Tindamax.
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
VESIcare is a brand name of solifenacin, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of VESIcare available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of VESIcare. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Class: Amphetamines
VA Class: CN801
CAS Number: 537-46-2
Brands: Desoxyn
High potential for abuse.a c
Administration of amphetamines for prolonged periods of time may lead to drug dependence and must be avoided.a b c
Particular attention should be paid to the possibility of individuals obtaining methamphetamine for nontherapeutic use or distribution to others, and the drug should be prescribed or dispensed sparingly.a c
Possible sudden death and serious cardiovascular events (e.g., fatal cardiorespiratory arrest), particularly in individuals who abuse methamphetamine.a c d (See Sudden Death and Serious Cardiovascular Events under Cautions.)
Dextrorotatory isomer of phenylmethylamine;a sympathomimetic amine with CNS-stimulating activity.c
Used as an adjunct to psychological, educational, social, and other remedial measures in the treatment of attention deficit hyperactivity disorder (ADHD) (hyperkinetic disorder, hyperkinetic syndrome of childhood, minimal brain dysfunction).a c e
Almost all studies comparing behavioral therapy versus stimulants alone have shown a much stronger therapeutic effect from stimulants than from behavioral therapy, and stimulants (e.g., amphetamines, methylphenidate) remain the drugs of choice for the management of ADHD.
Drug therapy is not indicated in all patients with ADHD, and such therapy should be considered only after a complete evaluation, including medical history, has been performed.a c
Use should depend on age and the clinician’s assessment of the severity and duration of symptoms and should not depend solely on one or more behavioral characteristics.a c
Not recommended for ADHD symptoms associated with acute stress reactions.a c
Has been used as an adjunct to caloric restriction in the short-term (i.e., a few weeks) treatment of exogenous obesity.a c However, because of limited efficacy (short-lived), such use no longer is recommended.
The anorexigenic effect appears to be temporary, seldom lasting more than a few weeks, and tolerance may occur.a b c
Obesity usually is a chronic disease, and short-term or intermittent therapy with anorexigenic drugs is unlikely to maintain long-term benefit.
Misuse and abuse have experienced a resurgence, in large part, due to the relative ease with which methamphetamine can be synthesized clandestinely from readily available chemicals such as ephedrine, phenylpropanolamine (no longer commercially available in the US), or pseudoephedrine. Recent restrictions (including enactment of the Comprehensive Methamphetamine Control Act of 1996, the Methamphetamine Anti-Proliferation Act [MAPA] of 2000, and the Combat Methamphetamine Epidemic Act [CMEA] of 2005) on the availability of these compounds are hoped to reverse this resurgence in misuse and abuse.
Administer orally.a c
When used as an anorexigenic agent, administer 30 minutes before each meal.c
Because of potential for insomnia, avoid administering doses in the late evening.a c
Available as methamphetamine hydrochloride; dosage expressed in terms of the salt.c
Adjust dosage according to individual response and tolerance; the smallest dose required to produce the desired response should always be used.a c
When possible, therapy should be interrupted occasionally to determine if there is a recurrence of behavioral symptoms sufficient to require continued treatment.a c
If tolerance to anorectic effect occurs, manufacturer suggests not to exceed recommended dosage (in an attempt to increase effect), but rather to discontinue therapy.c
Children ≥12 years of age: 5 mg given 30 minutes before each meal recommended by manufacturer.c Treatment should not exceed a few weeks.a c
Children ≥6 years of age: Initially, 5 mg once or twice daily; daily dosage is increased in 5-mg increments at weekly intervals until the optimum response is attained.a c
Usual dosage is 20–25 mg daily, given in 2 divided doses.a c
5 mg given 30 minutes before each meal recommended by manufacturer.c Treatment should not exceed a few weeks.a c
Children ≥12 years of age: Treatment should not exceed a few weeks.c
Treatment should not exceed a few weeks.c
No specific hepatic dosage recommendations.c
No specific renal dosage recommendations.c
Select dosage with caution, usually starting at the low end of the dosage range, because of age-related decreases in hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.a c
Contraindicated in patients with hypersensitivity or idiosyncrasy to sympathomimetic amines; in patients witha c symptomatic cardiovascular disease,a c hyperthyroidism,a c moderate to severe hypertension,a c glaucoma,a c or advanced arteriosclerosis;a c within 14 days of MAO inhibitor therapy;a c and in agitated patients.a c
Although amphetamines generally should not be used in patients with a history of drug abuse,a c some experts state that this is not an absolute contraindication, provided the patient can be monitored more carefully than would otherwise be indicated.
Sudden unexplained death, stroke, or MI reported in patients with or without structural cardiac abnormalities or other serious cardiac conditions receiving usual dosages of stimulants.c d f
Epidemiologic data suggest a possible association between use of stimulants and sudden unexplained death in healthy children and adolescents.g h i FDA unable to conclude that these data affect evaluation of overall risk and benefit of stimulants used to treat ADHD in children and adolescents.g FDA is conducting an ongoing safety review of amphetamines and other stimulants to evaluate possible link between use of these agents and sudden death in children.g h i Pediatric patients with ADHD and their parents should avoid discontinuing the child’s use of such stimulants before consulting a clinician.g
Thoroughly review medical history (including evaluation for family history of sudden death or ventricular arrhythmia) and perform physical examination in all children, adolescents, and adults being considered for stimulant therapy;c d if initial findings suggest presence of cardiac disease, perform further cardiac evaluation (e.g., ECG, echocardiogram).c
In general, avoid use of CNS stimulants in adults or children with known serious structural cardiac abnormalities, cardiomyopathy, serious heart rhythm abnormalities, CAD, or other serious cardiac conditions.c (See Contraindications under Cautions.)
Patients who develop exertional chest pain, unexplained syncope, or other symptoms suggestive of cardiac disease during stimulant treatment should undergo a prompt cardiac evaluation.c
Possible modest increases in average BP (i.e., by about 2–4 mm Hg) and heart rate (i.e., by about 3–6 bpm); larger increases may occur.c Modest increases not expected to have short-term sequelae; however, monitor all patients for larger changes in BP and heart rate.c
Caution advised in patients with underlying medical conditions that might be affected by increases in BP or heart rate (e.g., hypertension, heart failure, recent MI, ventricular arrhythmia).c
May exacerbate symptoms of behavior disturbance and thought disorder in patients with preexisting psychotic disorder.c
Psychotic symptoms (e.g., hallucinations, delusional thinking) may occur with usual dosages in children and adolescents without prior history of psychotic illness.c d If psychotic symptoms occur, consider causal relationship to stimulants, and discontinue therapy as appropriate.c
May precipitate mixed or manic episodes in ADHD patients with comorbid bipolar disorder; use with caution in these patients.c d Prior to initiating therapy, carefully screen patients with ADHD and comorbid depressive symptoms to identify risk for bipolar disorder; screening should include a detailed psychiatric history (e.g., family history of suicide, bipolar disorder, or depression).c
Manic symptoms may occur with usual dosages in children and adolescents without prior history of mania.c If manic symptoms occur, consider causal relationship to stimulants, and discontinue therapy as appropriate.c
Aggressive behavior and hostility (frequently observed in children and adolescents with ADHD) reported in patients receiving drug therapy for ADHD.c No systematic evidence that stimulants cause these adverse effects; however, monitor patients beginning treatment for ADHD for onset or worsening of aggressive behavior or hostility.c
Long-term (i.e., >14 months) administration expected to cause at least a temporary suppression of normal weight and/or height patterns in some children and adolescents.c
Manufacturer recommends monitoring growth during treatment; patients not growing or gaining weight as expected may require temporary discontinuance of treatment.c However, AAP states that studies of stimulants in children found little or no decrease in expected height, with any decrease in growth early in treatment being compensated for later on.
Possible lowering of seizure threshold in patients with history of seizures, in those with prior EEG abnormalities but no history of seizures, and, very rarely, in those without history of seizures and with no prior EEG abnormalities.c If seizures occur, discontinue therapy.c
Visual disturbances (difficulty with accommodation, blurred vision) reported with stimulants.a c
Least amount of methamphetamine feasible should be prescribed or dispensed at one time in order to minimize possible overdosage.c
Do not use to combat fatigue/exhaustion or to replace rest/sleep in normal persons.a c
Use with caution in patients with mild hypertension.a c Contraindicated in those with moderate or severe hypertension.c (See Contraindications under Cautions.)
Use with caution, if at all, in patients with hyperexcitability states or in those receiving drugs that may produce this effect.a Also use with caution in asthenic patients or in those with psychopathic personalities or history of suicidal or homicidal tendencies.a
Amphetamines reported to exacerbate motor and phonic tics and Tourette’s syndrome.c However, a history of tics or their development during therapy is not an absolute contraindication to continued use. Several controlled studies have not found stimulants to worsen or precipitate tics or Tourette’s syndrome. Nevertheless, evaluate for presence of tics and Tourette’s syndrome in children and their families prior to initiating stimulant therapy.c
Teratogenicity and embryolethality demonstrated in animals receiving high multiples of the human dose.c
Category C.c (See Fetal/Neonatal Morbidity and Mortality under Cautions.)
Risk of prematurity, low birth weight, and withdrawal symptoms (e.g., dysphoria, lassitude, agitation) in infants born to dependent women.c
Amphetamines are distributed into milk.a c Discontinue nursing or the drug.a c
Not recommended for treatment of ADHD in pediatric patients <6 years of age.f
Not recommended for management of exogenous obesity in pediatric patients <12 years of age.a b c
Aggressive behavior, hostility, and psychotic (e.g., hallucinations, delusional thinking) or manic symptoms reported in children and adolescents receiving stimulants for management of ADHD.b c (See Warnings under Cautions.)
Sudden death reported in children and adolescents with structural cardiac abnormalities or other serious cardiac conditions receiving usual dosages of stimulants.c Epidemiologic data also suggest a possible association between use of stimulants and sudden death in healthy children and adolescents.g h i (See Sudden Death and Serious Cardiovascular Events under Cautions.)
Long-term administration expected to cause at least a temporary suppression of normal weight and/or height patterns in some children and adolescents.a c (See Growth Suppression under Cautions.)
Insufficient experience in patients ≥65 years of age to determine whether geriatric patients respond differently than younger adults.a c Other clinical experience has not identified differences in responses between geriatric and younger patients.a c
Use with caution in geriatric or debilitated patients.a Select dosage with caution.a c (See Geriatric Patients under Dosage and Administration.)
Elevation of BP,c tachycardia,a c palpitations,a c dizziness,a c dysphoria,a c overstimulation,c insomnia,a c tremor,a c restlessness,a c headache,a c diarrhea,a c constipation,a c dry mouth,a c unpleasant taste,a c urticaria,a c impotence,a c changes in libido.a c
Drug or Test | Interaction | Comments |
|---|---|---|
Anesthetics, general (cyclopropane, halothane) | Possible increased sensitivity of heart to arrhythmic action of sympathomimetic aminesa | Avoid concomitant usea |
Antidepressants, tricyclic | Use concomitantly under close supervision; adjust dosage carefullya c | |
Insulin | Possible altered insulin requirements in patients with diabetes mellitusa c | Use concomitantly with caution in patients with diabetes mellitusa |
MAO inhibitors | Possible hypertensive crisisc | Contraindicated in patients currently or recently (within 14 days) receiving MAO inhibitora c |
Phenothiazines | Possible antagonism of CNS stimulant action of amphetaminesa c | |
Test for plasma corticosteroids | Amphetamines may substantially increase plasma corticosteroid concentrationsa c |
Readily and rapidly absorbed from the GI tract.a c
Therapeutic effects persist for 6–12 hours; effects may continue up to 24 hours following administration of large doses.a
Amphetamines apparently cross the placenta since withdrawal manifestations have occurred in neonates.c (See Pregnancy under Cautions.)
Amphetamines are distributed into milk.a c
Metabolized in the liver by aromatic hydroxylation, N-dealkylation, and deamination.a c
Excreted principally in urine.a With normal urinary pH, approximately 62% of the dose is excreted in urine within the first 24 hours as unchanged drug (about (1/3)) and metabolites (about (2/3)).a c
Excretion is enhanced in acidic urine.a c
4–5 hours.a c Alkaline urine substantially increases half-life.c
Tight, light-resistant containers at <30°C.a c f
Pharmacologic actions of methamphetamine are qualitatively similar to those of amphetamine and ephedrine and include CNS and respiratory stimulation and sympathomimetic activity including pressor response, mydriasis, bronchodilation, and contraction of the urinary bladder sphincter.a
CNS stimulating effect is approximately equal to or greater than that of amphetamine but less than that of dextroamphetamine; pressor effect is less than that of amphetamine but greater than that of ephedrine.a
Theories of dysfunction in ADHD focus on the prefrontal cortex, which controls many executive functions (e.g., planning, impulse control). Stimulants have putative effects on central dopamine and norepinephrine pathways that are crucial in frontal lobe function.
Produces an anorexigenic effect, leading to loss of weight.a c No primary effect on appetite has been demonstrated and it has been postulated that anorexigenic effects are secondary to increased sympathetic activity resulting from release of norepinephrine and dopamine.
Depresses motility of GI tract.a
Provide patient or caregiver with a copy of the manufacturer’s patient information (medication guide); discuss and answer questions about its contents as needed.a c d Instruct patient or caregiver to read and understand contents of medication guide before initiating therapy and each time the prescription is refilled.a c d f
Advise parents with concerns about long-term effects (e.g., effects on weight) and the need for continued therapy that drug holidays can be considered in consultation with the patient’s clinician. However, the benefits versus risks of such interruptions in therapy have not been established.
Advise not to increase or decrease dosage unless instructed by their clinician.c
Advise that abrupt discontinuance following prolonged administration of high dosages may result in extreme fatigue and mental depression.c
Question about possible substance abuse, including in family members (since they may abuse the patient’s medication supply).f
Advise patients to inform clinician immediately if adverse cardiovascular (e.g., chest pain, shortness of breath, fainting) or psychiatric effects (e.g., hallucinations, delusional thinking, mania) occur.f
Instruct about the potential for methamphetamine to impair patient’s ability to perform potentially hazardous activities, such as driving a vehicle or operating heavy machinery.a c f
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, dietary supplements, and herbal products, as well as any concomitant illnesses/conditions (e.g., cardiac/cardiovascular disease, thyroid disease, glaucoma, suicidal ideation or behaviors, mental/psychiatric disorder).c f
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.c f
Importance of informing patients of other important precautionary information.c (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Subject to control under the Federal Controlled Substances Act of 1970 as a schedule II (C-II) drug.a c
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
|---|---|---|---|---|
Oral | Tablets | 5 mg | Desoxyn ( C-II) | Ovation |
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 June 2010. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
a. AHFS drug information 2007. McEvoy GK, ed. Methamphetamine. Bethesda, MD: American Society of Health-System Pharmacists; 2007:2476-7.
b. AHFS drug information 2007. McEvoy GK, ed. Amphetamines general statement. Bethesda, MD: American Society of Health-System Pharmacists; 2007:2468-72.
c. Ovation Pharmaceuticals, Inc. Desoxyn (methamphetamine hydrochloride) tablets prescribing information. Deerfield, IL; 2007 May.
d. US Food and Drug Administration. FDA news: FDA directs ADHD drug manufacturers to notify patients about cardiovascular adverse events and psychiatric adverse events. Rockville, MD; 2007 Feb 21. From FDA website.
e. Ovation Pharmaceuticals, Inc., Deerfield, IL: Personal communication.
f. Ovation Pharmaceuticals, Inc. Desoxyn (methamphetamine hydrochloride) medication guide. Deerfield, IL; 2007 May.
g. Food and Drug Administration. FDA Alert: Information for healthcare professionals: Communication about an ongoing safety review of stimulant medications [dexmethylphenidate (marketed as Focalin, Focalin XR), dextroamphetamine (marketed as Dexedrine, Dexedrine Spansules, Dextrostat, and generics), lisdexamfetamine (marketed as Vyvanse), methamphetamine (marketed as Desoxyn), methylphenidate (marketed as Concerta, Daytrana, Metadate CD, Metadate ER, Methylin, Methylin ER, Ritalin, Ritalin-LA, and Ritalin-SR), mixed salts amphetamine (marketed as Adderall and Adderall XR), and pemoline (marketed as Cylert and generics)] used in children with attention-deficit/hyperactivity disorder (ADHD). Rockville, MD; 2009 Jun 23. From the FDA website.
h. Gould MS, Walsh BT, Munfakh JL et al. Sudden death and use of stimulant medications in youths. Am J Psychiatry. 2009; 166:992-1001. [PubMed 19528194]
i. Vitiello B, Towbin K. Stimulant treatment of ADHD and risk of sudden death in children. Am J Psychiatry. 2009; 166:955-7. [PubMed 19528196]
j. US Food and Drug Administration. AHRQ and FDA to collaborate in largest study ever of possible heart risks with ADHD medications. FDA News September 17, 2007. From FDA web site.
Cerezyme is a brand name of imiglucerase, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Cerezyme available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Cerezyme. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
L-Asparaginasa Filaxis may be available in the countries listed below.
Asparaginase is reported as an ingredient of L-Asparaginasa Filaxis in the following countries:
International Drug Name Search
Rozerem is a brand name of ramelteon, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Rozerem available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Rozerem. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
Yob may be available in the countries listed below.
Cefpodoxime is reported as an ingredient of Yob in the following countries:
International Drug Name Search
Rescriptor is a brand name of delavirdine, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of Rescriptor available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Rescriptor. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Treating moderate to severe psoriasis.
Alefacept is an immunosuppressant. It works by decreasing the activity of immune cells and decreasing the rate of skin cell multiplication.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Alefacept. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Alefacept. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Alefacept may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Alefacept as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Alefacept.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Dizziness; increased cough; muscle aches or pain; nausea; pain or swelling at the injection site; sore throat or throat inflammation.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; chills; fever; new or altered skin lesions or spots; painful or frequent urination; persistent sore throat; serious infections; swollen glands; unusual lumps; unusual vaginal discharge ; white patches in the mouth (oral thrush).
This is not a complete list of all side effects that may occur. If you have questions or need medical advice about side effects, contact your doctor or health care provider. You may report side effects to the FDA at 1-800-FDA-1088 (1-800-332-1088) or at http://www.fda.gov/medwatch.
See also: Alefacept side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org/DNN/), or emergency room immediately. Symptoms may include chills; headache; joint pain.
Store Alefacept at room temperature between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Keep in the original carton until ready for use. Once prepared, the diluted solution should be refrigerated at 36 to 46 degrees F (2 to 8 degrees C) and used within 4 hours. Check the expiration date on the label and properly discard any unused medicine after that time. Do not store in the bathroom. Keep Alefacept out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Alefacept. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
