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Index of reports
> Hospitalization (194)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Depakote (Divalproex) hospitalization. The selected reports were submitted to the FDA during the sample period of about a year.
Reports 1 - 30 of 194 Next >>
Possible Depakote side effects in 59 year old female
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-08-21
Patient: 59 year old female, weighing 83.5 kg (183.7 pounds)
Reactions: C-Reactive Protein Increased, Drug Interaction, Muscular Weakness, Rash Maculo-Papular, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: 750 mg, tid
Administration route: Oral
Indication: Bipolar Disorder
Lamotrigine
Dosage: 50 mg, bid
Administration route: Oral
Indication: Bipolar Disorder
Other drugs received by patient: Quetiapine; Hydroxychloroquine Sulfate; Aspirin; Simvastatin; Venlafaxine
Possible Depakote side effects in male
Reported by a health professional (non-physician/pharmacist) from France on 2012-08-21
Patient: male
Reactions: Abnormal Behaviour, Aggression
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Administration route: Oral
Indication: Product Used FOR Unknown Indication
End date: 2011-10-24
Equanil
Administration route: Oral
Indication: Product Used FOR Unknown Indication
End date: 2011-10-24
Exelon
Indication: Product Used FOR Unknown Indication
End date: 2011-01-01
Tiapridal
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Trimeprazine Tartrate
Administration route: Oral
Indication: Product Used FOR Unknown Indication
End date: 2011-10-24
Xanax
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Polyethylene Glycol; Digoxin
Possible Depakote side effects in male
Reported by a physician from United States on 2012-08-21
Patient: male
Reactions: White Blood Cell Count Decreased, Hospitalisation
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Keppra
Vimpat
Indication: Convulsion
Possible Depakote side effects in 59 year old female
Reported by a physician from United Kingdom on 2012-08-20
Patient: 59 year old female, weighing 83.5 kg (183.7 pounds)
Reactions: Drug Interaction, Muscular Weakness, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Administration route: Oral
Indication: Bipolar Disorder
Lamotrigine
Administration route: Oral
Indication: Bipolar Disorder
Other drugs received by patient: Simvastatin; Venlafaxine; Quetiapine; Aspirin; Hydroxychloroquine Sulfate
Possible Depakote side effects in 59 year old female
Reported by a physician from United Kingdom on 2012-08-20
Patient: 59 year old female, weighing 83.5 kg (183.7 pounds)
Reactions: Drug Interaction, Muscular Weakness, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Administration route: Oral
Indication: Bipolar Disorder
Lamotrigine
Administration route: Oral
Indication: Bipolar Disorder
Other drugs received by patient: Simvastatin; Quetiapine; Hydroxychloroquine Sulfate; Aspirin; Venlafaxine
Possible Depakote side effects in male
Reported by a consumer/non-health professional from Brazil on 2012-08-16
Patient: male
Reactions: Somnolence, Convulsion
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakene
Indication: Product Used FOR Unknown Indication
Start date: 2010-01-01
Depakote
Indication: Product Used FOR Unknown Indication
Start date: 2010-01-01
End date: 2010-01-01
Other drugs received by patient: Lamotrigine; Clobazam
Possible Depakote side effects in 59 year old female
Reported by a physician from United Kingdom on 2012-08-16
Patient: 59 year old female
Reactions: C-Reactive Protein Increased, Muscular Weakness, Drug Interaction, Rash Maculo-Papular, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Bipolar Disorder
Lamotrigine
Indication: Bipolar Disorder
Other drugs received by patient: Simvastatin; Hydroxychloroquine Sulfate; Quetiapine; Aspirin; Venlafaxine
Possible Depakote side effects in 59 year old female
Reported by a physician from United Kingdom on 2012-08-10
Patient: 59 year old female, weighing 83.5 kg (183.7 pounds)
Reactions: C-Reactive Protein Increased, Drug Interaction, Muscular Weakness, Rash Maculo-Papular, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: 2250mg per day
Administration route: Oral
Indication: Bipolar Disorder
Lamotrigine
Dosage: 100mg per day
Administration route: Oral
Indication: Bipolar Disorder
Other drugs received by patient: Hydroxychloroquine Sulfate; Venlafaxine; Simvastatin; Quetiapine; Aspirin
Possible Depakote side effects in
Reported by a physician from United States on 2012-08-09
Patient:
Reactions: White Blood Cell Count Decreased, Hospitalisation
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Keppra
Vimpat
Possible Depakote side effects in 59 year old female
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2012-08-09
Patient: 59 year old female, weighing 83.5 kg (183.7 pounds)
Reactions: Drug Interaction, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: 750 mg, 3 in 1 d, oral
Administration route: Oral
Indication: Bipolar Disorder
Lamotrigine
Dosage: 50 mg, 2 in 1 d, oral
Administration route: Oral
Indication: Bipolar Disorder
Other drugs received by patient: Venlafaxine HCL; Simvastatin; Quetiapine Fumarate; Hydroxychloroquine Sulfate; Aspirin
Possible Depakote side effects in female
Reported by a consumer/non-health professional from United States on 2012-08-09
Patient: female
Reactions: Weight Increased, Hospitalisation, Loss of Employment, Alopecia, Loss of Consciousness
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Possible Depakote side effects in female
Reported by a consumer/non-health professional from United States on 2012-08-08
Patient: female
Reactions: Agitation, Headache, Mania, Fatigue, Malaise, Hospitalisation, Anger, Depression, Tachyphrenia, Psychomotor Hyperactivity, Restlessness, Motor Dysfunction, Anxiety, Irritability, Panic Attack, Insomnia, Feeling Jittery, Feeling Abnormal
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Product Used FOR Unknown Indication
Klonopin
Dosage: drug use on and off for 21 years, upped from 1.5mg to 3mg daily
Indication: Mania
Klonopin
Indication: Bipolar Disorder
Klonopin
Other drugs received by patient: Restoril
Possible Depakote side effects in female
Reported by a lawyer from United States on 2012-08-08
Patient: female
Reactions: Cleft LIP, Conductive Deafness, Convulsion, Emotional Distress, Speech Disorder, Cleft Palate, Developmental Delay, Social Avoidant Behaviour, Otitis Media, Dacryostenosis Congenital, Attention Deficit / Hyperactivity Disorder, Eustachian Tube Dysfunction
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Foetal Exposure During Pregnancy
Topamax
Indication: Foetal Exposure During Pregnancy
Start date: 2004-11-24
End date: 2005-02-24
Other drugs received by patient: Multi-Vitamins; Synthroid
Possible Depakote side effects in female
Reported by a consumer/non-health professional from United States on 2012-08-06
Patient: female
Reactions: Cleft LIP, Emotional Distress, Speech Disorder, Cleft Palate, Social Avoidant Behaviour, Developmental Delay, Otitis Media, Dacryostenosis Congenital, Attention Deficit / Hyperactivity Disorder, Eustachian Tube Dysfunction
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Foetal Exposure During Pregnancy
Topamax
Indication: Foetal Exposure During Pregnancy
Start date: 2004-11-24
End date: 2005-02-24
Other drugs received by patient: Multi-Vitamins; Synthroid
Possible Depakote side effects in 61 year old male
Reported by a physician from United States on 2012-07-26
Patient: 61 year old male, weighing 76.2 kg (167.6 pounds)
Reactions: Lymphocyte Count Increased, Weight Decreased, Obsessive-Compulsive Disorder, Moderate Mental Retardation, Haematocrit Decreased, Granulocytopenia, Mean Cell Haemoglobin Concentration Increased, Thrombocytopenia, Oxygen Saturation Decreased, Lethargy, Hypotension, Pancytopenia, Deafness Neurosensory, Cognitive Disorder, Monocyte Count Increased, Haemoglobin Decreased, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: 1500 mg, bid
Indication: Schizoaffective Disorder
End date: 2011-12-03
Fanapt
Dosage: 12 mg, bid
Administration route: Oral
Indication: Schizoaffective Disorder
Start date: 2011-03-01
End date: 2011-12-03
Other drugs received by patient: Ammonium Lactate; Gabapentin; Gabapentin; Loperamide; Metformin Hydrochloride; Tear Drop; Eucerin Creme; Famotidine; Hydrocodone Bitartrate and Acetaminophen; Iloperidone; Levothyroxine Sodium; BEN GAY; Fenofibrate; Selenium Sulfide; Divalproex Sodium; Famotidine; Gabapentin; Levothyroxine Sodium; Metformin Hydrochloride; Bisacodyl; Iloperidone; Fenofibrate; Gabapentin; Acetaminophen; Benztropine Mesylate; Calcium Carbonate W / Vitamin D NOS; Zinc Oxide Ointment
Possible Depakote side effects in 61 year old male
Reported by a pharmacist from United States on 2012-07-25
Patient: 61 year old male, weighing 168.0 kg (369.6 pounds)
Reactions: Lymphocyte Count Increased, Weight Decreased, Obsessive-Compulsive Disorder, Moderate Mental Retardation, Nutritional Condition Abnormal, Haematocrit Decreased, RED Blood Cell Count Decreased, Mean Cell Haemoglobin Concentration Increased, Thrombocytopenia, Oxygen Saturation Decreased, Lethargy, White Blood Cell Count Decreased, Hypotension, Deafness Neurosensory, Monocyte Count Increased, Cognitive Disorder, Haemoglobin Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: 1500 mg, bid
Administration route: Oral
Indication: Schizoaffective Disorder
Fanapt
Dosage: 12 mg, bid
Administration route: Oral
Indication: Schizoaffective Disorder
Start date: 2011-03-01
Other drugs received by patient: Gabapentin; Bengay Ultra Strength CRM; Benztropine Mesylate; Hydrocodone; Benztropine Mesylate; Gabapentin; Gabapentin; Famotidine; Gabapentin; Levothyroxine Sodium; Divalproex Sodium; Iloperidone; Divalproex Sodium; Famotidine; Iloperidone; Metformin Hydrochloride
Possible Depakote side effects in 43 year old male
Reported by a health professional (non-physician/pharmacist) from France on 2012-07-24
Patient: 43 year old male
Reactions: Cytolytic Hepatitis, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms, Toxic Skin Eruption
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Other drugs received by patient: Ditropan; Foradil; Tegretol; Imovane; Theralene; Pulmicort; Loxapine HCL; Ciprofloxacin HCL
Possible Depakote side effects in female
Reported by a consumer/non-health professional from Japan on 2012-07-24
Patient: female
Reactions: Blood Pressure Increased, Weight Decreased, Blood Count Abnormal, Cystitis, Loss of Consciousness, Burning Sensation, Palpitations, Ingrowing Nail, Cholecystectomy, Abdominal Distension, Arteriosclerosis Coronary Artery, TOE Operation
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Atacand
Dosage: 32 mg, unk
Indication: Product Used FOR Unknown Indication
Avapro
Indication: Hypertension
Bactrim
Indication: Product Used FOR Unknown Indication
Benicar
Dosage: unk
Administration route: Oral
Indication: Hypertension
Start date: 2007-01-01
Bystolic
Indication: Product Used FOR Unknown Indication
Cardizem
Indication: Product Used FOR Unknown Indication
Cipro
Indication: Product Used FOR Unknown Indication
Depakote
Dosage: unk
Indication: Convulsion
Start date: 1996-01-01
Dilantin
Dosage: unk
Indication: Product Used FOR Unknown Indication
Start date: 1996-01-01
Diovan
Indication: Product Used FOR Unknown Indication
Furosemide
Indication: Product Used FOR Unknown Indication
Hydrochlorothiazide
Indication: Product Used FOR Unknown Indication
Levaquin
Indication: Product Used FOR Unknown Indication
Lidocaine
Dosage: unk
Indication: Anaesthesia
Start date: 2010-05-13
End date: 2010-05-13
Lisinopril
Indication: Product Used FOR Unknown Indication
Losartan Potassium
Indication: Product Used FOR Unknown Indication
Macrobid
Indication: Product Used FOR Unknown Indication
Norvasc
Dosage: 5 mg, bid
Administration route: Oral
Start date: 2010-01-01
Norvasc
Dosage: 5 mg/daily
Administration route: Oral
Start date: 1997-01-01
Norvasc
Dosage: 2.5 mg/daily
Administration route: Oral
Indication: Hypertension
Start date: 1995-01-01
Reglan
Indication: Product Used FOR Unknown Indication
Xanax
Dosage: 0.5 df/day
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Levothyroxine Sodium; Clonidine
Possible Depakote side effects in 6 year old male
Reported by a pharmacist from United States on 2012-07-20
Patient: 6 year old male, weighing 22.0 kg (48.4 pounds)
Reactions: Pancreatitis Acute, Thirst, Pyrexia, Haemoglobin Decreased, Ileus, Pancreatic Pseudocyst, Hypoxia, Pleural Effusion, Pancreatitis Haemorrhagic
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Possible Depakote side effects in
Reported by a individual with unspecified qualification from United States on 2012-07-17
Patient:
Reactions: Circumstance or Information Capable of Leading To Medication Error, Wrong Drug Administered, Drug Dispensing Error
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Depakote
Possible Depakote side effects in 57 year old female
Reported by a health professional (non-physician/pharmacist) from France on 2012-07-10
Patient: 57 year old female
Reactions: Mixed Liver Injury
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Ceftriaxone
Indication: Lung Disorder
Start date: 2012-03-09
End date: 2012-03-15
Depakote
Administration route: Oral
Start date: 2012-03-13
End date: 2012-03-19
Depakote
Administration route: Oral
Indication: Mania
Start date: 2012-03-09
End date: 2012-03-12
Other drugs received by patient: Atarax; Solian
Possible Depakote side effects in male
Reported by a physician from United States on 2012-07-09
Patient: male, weighing 147.9 kg (325.3 pounds)
Reactions: Fatigue, Adverse Event, Abnormal Behaviour, Dizziness
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Product Used FOR Unknown Indication
Lithium Carbonate
Indication: Product Used FOR Unknown Indication
Risperdal
Dosage: 2 mg in am and 4 mg in pm
Administration route: Oral
End date: 1997-01-01
Risperdal
Dosage: 2 mg in am and 4 mg in pm
Administration route: Oral
End date: 2012-01-01
Risperdal
Dosage: 2 mg in am and 4 mg in pm
Administration route: Oral
Indication: Psychotic Behaviour
End date: 1987-01-01
Risperidone
Indication: Product Used FOR Unknown Indication
Topamax
Administration route: Oral
Indication: Product Used FOR Unknown Indication
End date: 2012-01-01
Topiramate
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Possible Depakote side effects in 52 year old male
Reported by a health professional (non-physician/pharmacist) from France on 2012-07-09
Patient: 52 year old male
Reactions: Pancreatitis Acute, Circulatory Collapse, Respiratory Distress
Adverse event resulted in: life threatening event, hospitalization
Drug(s) suspected as cause:
Aspirin
Administration route: Oral
Indication: Cerebrovascular Accident
Baclofen
Indication: Cerebrovascular Accident
Depakote
Administration route: Oral
Indication: Epilepsy
End date: 2012-02-28
Diprivan
Indication: Anaesthesia
Start date: 2012-02-27
End date: 2012-02-27
Pipamperone
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Possible Depakote side effects in female
Reported by a physician from United Kingdom on 2012-07-03
Patient: female
Reactions: Mania, Mental Impairment, Psychotic Disorder, Dysphagia, Sedation, Thyroid Disorder
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: 1500 mg
Depakote
Dosage: 1000 mg
Indication: Bipolar Disorder
Lithium Carbonate
Indication: Bipolar Disorder
NEO-Mercazole TAB
Dosage: 20 mg
Indication: Bipolar Disorder
Olanzapine
Indication: Bipolar Disorder
Quetiapine Fumarate
Dosage: 750 mg
Quetiapine Fumarate
Dosage: 300 mg
Indication: Bipolar Disorder
Possible Depakote side effects in
Reported by a consumer/non-health professional from United States on 2012-07-02
Patient:
Reactions: Anxiety, Cardiac Flutter, Atrial Fibrillation
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Depakote
Possible Depakote side effects in 58 year old female
Reported by a consumer/non-health professional from United States on 2012-07-02
Patient: 58 year old female, weighing 162.0 kg (356.4 pounds)
Reactions: Mania, Weight Increased, Vitamin D Decreased, Mental Disorder, Weight Fluctuation, Paraesthesia, Thyroid Function Test Abnormal
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Mania
Start date: 1998-01-01
Depakote
Indication: Bipolar Disorder
Start date: 1998-01-01
Depakote
Indication: Mania
Start date: 2005-01-01
Depakote
Indication: Bipolar Disorder
Start date: 2005-01-01
Lithium Carbonate
Dosage: 300 mg; bid,po
Administration route: Oral
Indication: Mania
Start date: 2012-06-08
Lithium Carbonate
Dosage: 300 mg; bid,po
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2012-06-08
Lithium Carbonate
Indication: Mania
Start date: 1998-01-01
Lithium Carbonate
Indication: Bipolar Disorder
Start date: 1998-01-01
Lithium Carbonate
Indication: Mania
Start date: 1995-01-01
Lithium Carbonate
Indication: Bipolar Disorder
Start date: 1995-01-01
Other drugs received by patient: Clonazepam; Seroquel
Possible Depakote side effects in 32 year old female
Reported by a physician from France on 2012-06-30
Patient: 32 year old female
Reactions: Intentional Overdose, Hyperammonaemia, Miosis, Tachycardia, Suicide Attempt, Toxicity To Various Agents, Hypokalaemia, Loss of Consciousness
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Dosage: ingested 50 enteric-coated tablets of valproic acid 500mg
Indication: Suicide Attempt
Olanzapine
Dosage: ingested unknown amount of olanzapine
Possible Depakote side effects in female
Reported by a consumer/non-health professional from France on 2012-06-29
Patient: female
Reactions: Abdominal Pain, Weight Decreased, Urinary Incontinence, Blood Count Abnormal, Headache, Loss of Consciousness, Palpitations, Feeling Hot, Ingrowing Nail, Gallbladder Disorder, Nervousness, Anaemia, Hypoaesthesia, Gastric Disorder, Convulsion, Insomnia, Cholecystectomy, Platelet Count Decreased, Drug Ineffective, Blood Triglycerides Increased, Drug Interaction, Micturition Frequency Decreased, Fall, Arterial Occlusive Disease, Dizziness, TOE Operation, Kidney Infection, Blood Pressure Increased, Lung Neoplasm, Cystitis, Arteriogram Coronary Abnormal, Full Blood Count Decreased, Burning Sensation, Carbuncle, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Atacand
Dosage: 32 mg, unk
Administration route: Oral
Indication: Renal Disorder
Start date: 1995-01-01
Avapro
Dosage: unk
Indication: Hypertension
Bactrim
Dosage: unk
Indication: Product Used FOR Unknown Indication
Benicar
Dosage: unk
Administration route: Oral
Indication: Hypertension
Start date: 2007-01-01
Cardizem
Dosage: unk
Indication: Product Used FOR Unknown Indication
Ciprofloxacin HCL
Dosage: unk
Indication: Product Used FOR Unknown Indication
Depakote
Dosage: unk
Indication: Convulsion
Start date: 1995-01-01
End date: 2004-01-01
Dilantin
Dosage: unk
Indication: Convulsion
Start date: 1995-01-01
Diovan
Dosage: unk
Indication: Product Used FOR Unknown Indication
Furosemide
Dosage: 20 mg, unk
Indication: Product Used FOR Unknown Indication
Furosemide
Dosage: unk
Hydrochlorothiazide
Dosage: unk
Indication: Product Used FOR Unknown Indication
Start date: 2011-03-07
Levaquin
Dosage: unk
Indication: Product Used FOR Unknown Indication
Lidocaine
Dosage: unk
Indication: Anaesthesia
Start date: 2010-05-13
End date: 2010-05-13
Lisinopril
Dosage: unk
Indication: Product Used FOR Unknown Indication
Losartan Potassium
Dosage: unk
Indication: Product Used FOR Unknown Indication
Macrobid
Dosage: unk
Indication: Product Used FOR Unknown Indication
Nebivolol
Dosage: unk
Indication: Product Used FOR Unknown Indication
Nopalea
Dosage: unk
Indication: Musculoskeletal Pain
Start date: 2010-01-01
Nopalea
Indication: Blood Triglycerides Increased
Norvasc
Dosage: 2.5 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 1994-01-01
Norvasc
Dosage: 0.5 mg, unk
Administration route: Oral
Norvasc
Dosage: 2.5 mg, unk
Administration route: Oral
Start date: 2010-07-19
End date: 2010-07-21
Norvasc
Dosage: 0.5 mg, unk
Administration route: Oral
Start date: 2010-07-22
Norvasc
Dosage: 5 mg, bid
Administration route: Oral
Start date: 2010-01-01
Norvasc
Dosage: 5 mg/day
Administration route: Oral
End date: 1997-01-01
Reglan
Dosage: unk
Indication: Product Used FOR Unknown Indication
Toprol-XL
Dosage: 25 mg/day
Administration route: Oral
Indication: Heart Rate Abnormal
Toprol-XL
Indication: Flushing
Xanax
Dosage: 0.5 mg/day
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Nitroglycerin; Clonidine; Metoprolol Succinate; Ascorbic Acid; Levothyroxine Sodium
Possible Depakote side effects in 67 year old female
Reported by a pharmacist from United States on 2012-06-28
Patient: 67 year old female
Reactions: Granulocytopenia, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Clozapine
Indication: Psychotic Disorder
End date: 2012-01-01
Clozapine
Clozapine
Clozapine
Clozapine
Clozapine
Indication: Depression
End date: 2012-01-01
Clozapine
Clozapine
Clozapine
Indication: Bipolar Disorder
End date: 2012-01-01
Depakote
End date: 2012-01-01
Possible Depakote side effects in female
Reported by a consumer/non-health professional from United States on 2012-06-28
Patient: female, weighing 58.1 kg (127.8 pounds)
Reactions: Movement Disorder, Cardiac Discomfort, Drug Ineffective, Sensory Loss, Weight Increased, Eye Disorder, Hypersomnia, Blood Pressure Increased, Dyspnoea, Ill-Defined Disorder, Anxiety, Middle Insomnia, Panic Attack, Activities of Daily Living Impaired, Asthenia, Blindness, Feeling Abnormal
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Depakote
Indication: Product Used FOR Unknown Indication
Klonopin
Indication: Product Used FOR Unknown Indication
Neurontin
Indication: Product Used FOR Unknown Indication
Trazodone HCL
Indication: Product Used FOR Unknown Indication
Vistaril
Administration route: Oral
Indication: Product Used FOR Unknown Indication
Other drugs received by patient: Seroquel; Strattera
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