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Zarontin  Zarontin

 Zarontin Product Name :  Zarontin
Product Type :  Ethosuximide
Packaging and Product :  250mg Capsules in Bottles of 200 Capsules
Manufacturer :  Parke Davis

 Zarontin: Manufacturers Information Sheet
 Zarontin: Manufacturers Information Sheet for Patients

** We are no longer supplying this product.


Zarontin is an anticonvulsant used for the control of absence (petit mal) epilepsy.

Contraindications

Ethosuximide should not be used in patients with a history of hypersensitivity to succinimides.

Precautions

Blood dyscrasias, including some with fatal outcome, have been reported to be associated with the use of ethosuximide; therefore, periodic blood counts should be performed. Ethosuximide is capable of producing morphological and functional changes in the animal liver. In humans, abnormal liver and renal function studies have been reported. Administer ethosuximide with extreme caution to patients with known liver or renal disease. Periodic urinalysis and liver function studies are advised for all patients receiving the drug. Cases of systemic lupus erythematosus have been reported with the use of ethosuximide. The physician should be alert to this possibility.

Ethosuximide may impair the mental and/or physical abilities required for the performance of potentially hazardous tasks, such as driving a motor vehicle or other such activity requiring alertness; therefore, caution the patient accordingly.

Ethosuximide, when used alone in mixed types of epilepsy, may increase the frequency of generalized tonic-clonic attacks in some patients.

Proceed slowly when increasing or decreasing dosage, as well as when adding or eliminating other medication. Abrupt withdrawal of anticonvulsant medication may precipitate petit mal status.

Adverse Side Effects

Gastrointestinal - Gastrointestinal symptoms occur frequently and include anorexia, vague gastric upset, nausea and vomiting, cramps, epigastric and abdominal pain, weight loss, and diarrhea.

Hemopoietic - Leukopenia, agranulocytosis, pancytopenia, aplastic anemia, eosinophilia.

Nervous system - Neurologic and sensory reactions reported during therapy with ethosuximide have included drowsiness, headache, dizziness, euphoria, hiccups, irritability, hyperactivity, lethargy, fatigue, and ataxia. Psychiatric or psychological aberrations associated with ethosuximide administration have included disturbances of sleep, night terrors, inability to concentrate, and aggressiveness. These effects may be noted particularly in patients who have previously exhibited psychological abnormalities. There have been rare reports of paranoid psychosis, increased libido, and increased state of depression with overt suicidal intentions.

Integumentary - Dermatologic manifestations which have occurred with the administration of ethosuximide have included urticaria, Stevens-Johnson syndrome, systemic lupus erythematosus, and pruritic erythematous rashes.

Genitourinary - Microscopic hematuria.

Miscellaneous - Myopia, vaginal bleeding, swelling of the tongue, gum hypertrophy, hirsutism.

 

 

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