Generic Name: Depakote
What is Depakote?
There are in vitro studies that suggest valproate stimulates the replication of the HIV and CMV viruses under certain experimental conditions.
The clinical consequence, if any, is not known. Additionally, the relevance of these in vitro findings is uncertain for patients receiving maximally suppressive antiretroviral therapy. Nevertheless, these data should be borne in mind when interpreting the results from regular monitoring of the viral load in HIV infected patients receiving valproate or when following CMV infected patients clinically.
There have been rare reports of medication residue in the stool. Some patients have had anatomic including ileostomy or colostomy or functional gastrointestinal disorders with shortened GI transit times. In some reports, medication residues have occurred in the context of diarrhea. It is recommended that plasma valproate levels be checked in patients who experience medication residue in the stool, and patients' clinical condition should be monitored.
If clinically indicated, alternative treatment may be considered. Advise the patient to read the FDA-approved patient labeling Medication Guide. Inform pregnant women and women of childbearing potential that use of valproate during pregnancy increases the risk of birth defects and decreased IQ in children who were exposed.
Advise women to use effective contraception while using valproate.
Monotherapy Initial Therapy Depakote has not been systematically studied as initial therapy. Depakote is indicated for prophylaxis of migraine headaches in adults. Dosing in Elderly Patients Due to a decrease in unbound clearance of valproate and possibly a greater sensitivity to somnolence in the elderly, the starting dose should be reduced in these patients. Dose-Related Adverse Reactions The frequency of adverse effects particularly elevated liver enzymes and thrombocytopenia may be dose-related.
Irritation Patients who experience G. Complex Partial SeizuresFor adults and children 10 years of age or older. Monotherapy Initial Therapy Depakote ER has not been systematically studied as initial therapy.
Dose-Related Adverse ReactionsThe frequency of adverse effects particularly elevated liver enzymes and thrombocytopenia may be dose-related. IrritationPatients who experience G. CompliancePatients should be informed to take Depakote ER every day as prescribed.
EpilepsyDEPAKOTE tablets are administered orally.
How should I take Depakote?
Keppra might impair your cognitive functioning and thinking. Be watchful if you drive or do anything that requires you to be alert. Inform your doctor if you are pregnant or plan to become pregnant while using this medication. Do not start or stop taking Keppra during pregnancy without consulting your doctor first.
Having a seizure during pregnancy could harm both the unborn baby and mother. Seizure control is very crucial during pregnancy and the advantages of preventing seizures may outweigh any risks posed by using Keppra.
What should I avoid while taking Depakote?
Overdose If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call 911. NotesDo not share this medication with others. Missed DoseIf you miss a dose, take it as soon as you remember. StorageStore at room temperature away from light and moisture. Add to Cabinet Add Adderall to my medicine cabinet. I amCurrently Taking Researching Previously TakenReason for takingAttention Deficit Disorder with Hyperactivity Recurring Sleep Episodes During the Day Other Did you know.
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Depakote side effects
My question is relating to the Depakote which she takes. I have read that Depakote can cause interference with thyroid function tests but have not been able to find any information as how it can affect the test. The individual I work with is also on Synthroid and I am curious if she may be on this medication and may not really need it.
Do you have any information. Answer: I don't know of any interaction between Depakote and the thyroid.
Common Depakote ide effects may include:
Inflammation of your pancreas that can cause death.
You may take this medicine with food or on an empty stomach.
Research has been found that suicidal thoughts and actions are up to two times more common in people who have not taken Depakote or another similar anticonvulsant.
This is not health insurance.
What should I discuss with my healthcare provider before taking divalproex sodium Depakote, Depakote ER, Depakote Sprinkles. How should I take divalproex sodium Depakote, Depakote ER, Depakote Sprinkles. What happens if I miss a dose Depakote, Depakote ER, Depakote Sprinkles.
Where can I get more information?
Approximately half of these patients had treatment discontinued, with return of platelet counts to normal.
Problems with white blood cell count and blood platelets, which can also be severe, may also develop on this medication.