Ülke: ABD
Dil: İngilizce
Kaynak: NLM (National Library of Medicine)
DIVALPROEX SODIUM (UNII: 644VL95AO6) (VALPROIC ACID - UNII:614OI1Z5WI)
State of Florida DOH Central Pharmacy
DIVALPROEX SODIUM
VALPROIC ACID 500 mg
ORAL
PRESCRIPTION DRUG
Divalproex sodium extended-release tablets are a valproate and are indicated for the treatment of acute manic or mixed episodes associated with bipolar disorder, with or without psychotic features. A manic episode is a distinct period of abnormally and persistently elevated, expansive, or irritable mood. Typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, poor judgment, aggressiveness, and possible hostility. A mixed episode is characterized by the criteria for a manic episode in conjunction with those for a major depressive episode (depressed mood, loss of interest or pleasure in nearly all activities). The efficacy of divalproex sodium extended-release tablets is based in part on studies of divalproex sodium delayed-release tablets in this indication, and was confirmed in a 3-week trial with patients meeting DSM-IV TR criteria for bipolar I disorder, manic or mixed type, who were hospitalized for acute mania [see Clinical Studies (
Divalproex Sodium Extended-release Tablets, USP are available containing divalproex sodium, USP equivalent to 250 mg or 500 mg of valproic acid. The 250 mg tablets are white, film-coated, round, unscored tablets debossed with M over 177 on one side of the tablet and blank on the other side. The 500 mg tablets are white, film-coated, oval, unscored tablets debossed with M 473 on one side of the tablet and blank on the other side. They are supplied by State of Florida DOH Central Pharmacy as follows: Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.] PHARMACIST: Dispense a Medication Guide with each prescription. * Maalox® is a registered trademark of Novartis. † TitralacTM is a trademark of 3M.
Abbreviated New Drug Application
DIVALPROEX SODIUM - DIVALPROEX SODIUM TABLET, FILM COATED, EXTENDED RELEASE State of Florida DOH Central Pharmacy ---------- MEDICATION GUIDE DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP (dye val′ proe ex soe′ dee um) 250 mg and 500 mg Read this Medication Guide before you start taking divalproex sodium extended-release tablets and each time you get a refill. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or treatment. What is the most important information I should know about divalproex sodium extended-release tablets? Do not stop taking divalproex sodium extended-release tablets without first talking to your healthcare provider. Stopping divalproex sodium extended-release tablets suddenly can cause serious problems. Divalproex sodium extended-release tablets can cause serious side effects, including: 1. Serious liver damage that can cause death, especially in children younger than 2 years old. The risk of getting this serious liver damage is more likely to happen within the first 6 months of treatment. Call your healthcare provider right away if you get any of the following symptoms: • nausea or vomiting that does not go away • loss of appetite • pain on the right side of your stomach (abdomen) • dark urine • swelling of your face • yellowing of your skin or the whites of your eyes In some cases, liver damage may continue despite stopping the drug. 2. Divalproex sodium extended-release tablets may harm your unborn baby. • If you take divalproex sodium extended-release tablets during pregnancy for any medical condition, your baby is at risk for serious birth defects. The most common birth defects with divalproex sodium extended-release tablets affect the brain and spinal cord and are called spina bifida or neural tube defects. These defects occur in 1 to 2 out of every 100 babies born to mothers who use this medicine during pregnancy. These defects can begin in the first month, even before you know yo Belgenin tamamını okuyun
DIVALPROEX SODIUM - DIVALPROEX SODIUM TABLET, FILM COATED, EXTENDED RELEASE STATE OF FLORIDA DOH CENTRAL PHARMACY ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS. DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP FOR ORAL USE INITIAL U.S. APPROVAL: 2000 WARNING: LIFE THREATENING ADVERSE REACTIONS _SEE FULL PRESCRIBING INFORMATION FOR COMPLETE BOXED WARNING_ • • • • RECENT MAJOR CHANGES Boxed Warning, Fetal Risk 06/2013 Indications and Usage, Important Limitations (1.4) 06/2013 Contraindications (4) 06/2013 Warnings and Precautions, Birth Defects (5.2) 06/2013 Warnings and Precautions, Decreased IQ (5.3) 06/2013 Warnings and Precautions, Use in Women of Childbearing Potential (5.4) 06/2013 Warning and Precautions, Medication Residue in the Stool (5.18) 02/2013 INDICATIONS AND USAGE Divalproex sodium extended-release tablets are an anti-epileptic drug indicated for: • • • DOSAGE AND ADMINISTRATION • • • • • DOSAGE FORMS AND STRENGTHS Tablets: 250 mg and 500 mg (3) CONTRAINDICATIONS • • • HEPATOTOXICITY, INCLUDING FATALITIES, USUALLY DURING FIRST 6 MONTHS OF TREATMENT. CHILDREN UNDER THE AGE OF 2 YEARS ARE AT CONSIDERABLY HIGHER RISK OF FATAL HEPATOTOXICITY. MONITOR PATIENTS CLOSELY, AND PERFORM LIVER FUNCTION TESTS PRIOR TO THERAPY AND AT FREQUENT INTERVALS THEREAFTER (5.1) TERATOGENICITY, INCLUDING NEURAL TUBE DEFECTS (5.2) FETAL RISK, PARTICULARLY NEURAL TUBE DEFECTS, OTHER MAJOR MALFORMATIONS, AND DECREASED IQ (5.2, 5.3, 5.4 ) PANCREATITIS, INCLUDING FATAL HEMORRHAGIC CASES (5.3) Acute treatment of manic or mixed episodes associated with bipolar disorder, with or without psychotic features (1.1) Monotherapy and adjunctive therapy of complex partial seizures and simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include absenc Belgenin tamamını okuyun