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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Depacon (Valproate). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view all available reports.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (5)
Cases resulting in a serious event (5)
Cases resulting in death (1)
Cases resulting in life threatening events (1)
Cases resulting in hospitalization (4)
Cases resulting in disability (1)
Cases resulting in other serious reactions (2)
Adverse event in 17 year old female receiving Depacon (Valproate)
Reported by a pharmacist from United States on 2007-10-16
Patient: 17 year old female, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Encephalopathy
Adverse event resulted in: hospitalization
Suspect drug(s):
Depacon (Valproate)
Adverse event in female receiving Depacon (Valproate)
Reported by a physician from United States on 2007-07-02
Patient: female
Adverse reactions / side effects: Thrombocytopenia
Adverse event resulted in: death
Suspect drug(s):
Keppra
Indication: Headache
Depacon
Adverse event in 37 year old male receiving Depacon (Valproate)
Reported by a physician from United States on 2007-06-19
Patient: 37 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Appendicitis Perforated, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Depakote
Administration route: Oral
Indication: Convulsion
End date: 2007-05-01
Depacon
Indication: Convulsion
Start date: 2007-05-01
End date: 2007-05-01
Adverse event in 57 year old male receiving Depacon (Valproate)
Reported by a consumer/non-health professional from United States on 2007-05-30
Patient: 57 year old male, weighing 113.4 kg (249.5 pounds)
Adverse reactions / side effects: Mania, Oedema Peripheral, Urticaria, Mental Disorder, Toxic Epidermal Necrolysis, Aggression
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Depacon
Dosage: iv
Indication: Mania
Start date: 2005-12-05
End date: 2005-12-05
Depacon
Dosage: iv
Indication: Psychotic Disorder
Start date: 2005-12-05
End date: 2005-12-05
Adverse event in male receiving Depacon (Valproate)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-04
Patient: male
Adverse reactions / side effects: Drug Level Increased, Encephalopathy, Tonic Clonic Movements, Status Epilepticus, Somnolence, Apraxia, Platelet Count Decreased, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Depakene
Administration route: Oral
Indication: Partial Seizures
Start date: 2007-03-12
End date: 2007-03-15
Depakene
Administration route: Oral
Depacon
Indication: Partial Seizures
Start date: 2007-03-08
Depacon
End date: 2007-03-12
Levetiracetam
Administration route: Oral
Indication: Partial Seizures
Start date: 2007-03-09
End date: 2007-03-10
Levetiracetam
Administration route: Oral
Indication: Status Epilepticus
Start date: 2007-03-11
End date: 2007-03-12
Other drugs received by patient: Pantoprazole; Fluconazole; Mianserin Hydrochloride; Pefloxacin Mesilate; Pefloxacin Mesilate; Acenocoumarol; Acebutolol; Finasteride; Prazepam; Diantalvic; Trimetazidine Hydrochloride; Furosemide
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