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Fosrenol Side Effects Report #5657774-1
Physician from BELGIUM reported FOSRENOL problem on Feb 26, 2008. Female patient, 64 years of age, weighting 133.4 lb, was diagnosed with hyperphosphataemia and was treated with FOSRENOL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, depressed level of consciousness, fatigue, stupor, . FOSRENOL dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE, TEMESTA. Patient was hospitalized. Patient recovered.

Valproic Side Effects Report #5662526-2
VALPROIC ACID problem was reported by a Pharmacist from UNITED STATES on Mar 10, 2008. Male patient, 52 years of age, weighting 209.4 lb, was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: ammonia increased, fall, gait disturbance, . VALPROIC ACID dosage: 2500 MG DAILY PO. During the same period patient was treated with HALOPERIDOL. Patient recovered.

Topiramate Side Effects Report #5672609-9
Physician from UKRAINE reported TOPIRAMATE problem on Mar 02, 2007. Female patient, weighting 16.53 lb, was diagnosed with partial seizures and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, varicella, . TOPIRAMATE dosage: unknown. During the same period patient was treated with DEPAKENE. Patient was hospitalized. Patient recovered.

Altace Side Effects Report #5674537-1
ALTACE problem was reported by a Consumer or non-health professional from ITALY on Mar 11, 2008. Female patient was diagnosed with nephrotic syndrome and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, coma, hepatic encephalopathy, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with INDERAL, KANRENOL, LOSEC, LORTAAN, PORTOLAC, LASIX. Patient was hospitalized. Patient recovered.


Forteo Side Effects Report #5689260-7
Physician from UNITED STATES reported FORTEO problem on Mar 21, 2008. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: ammonia increased, anxiety, aspartate aminotransferase increased, asthenia, bilirubin conjugated increased, blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, blood calcium decreased, . FORTEO dosage: unknown. During the same period patient was treated with FUROSEMIDE, PREVACID, SPIRONO, EFFEXOR, COMBIVENT, LORATADINE, PANCRELIPASE, NYSTATIN. Patient was hospitalized and became disabled. Patient died on 11/30/2007.

Valproic Side Effects Report #5620913-2
VALPROIC ACID problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Male patient, 27 years of age, was diagnosed with bipolar disorder and was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: ammonia increased, completed suicide, electroencephalogram abnormal, hypoxia, no therapeutic response, oliguria, overdose, . VALPROIC ACID dosage: unknown. During the same period patient was treated with LITHIUM CARBONATE. Patient died.

Valproic Side Effects Report #5623302-X
Physician from UNITED STATES reported VALPROIC ACID problem on Jan 07, 2008. Male patient, 27 years of age, was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: ammonia increased, anion gap increased, blood pressure diastolic decreased, calcium ionised decreased, completed suicide, hypothermia, hypoxia, miosis, . VALPROIC ACID dosage: unknown. Patient was hospitalized. Patient died.

Cubicin Side Effects Report #5624726-7
CUBICIN problem was reported by a Pharmacist from UNITED STATES on Jan 24, 2008. Female patient, weighting 119.9 lb, was diagnosed with cellulitis and was treated with CUBICIN. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood creatine phosphokinase increased, myoglobin urine present, renal failure acute, respiratory failure, . CUBICIN dosage: 500 MG;QD;IV. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5625006-6
Health Professional from FINLAND reported REBIF problem on Jan 24, 2008. Male patient, 34 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: ammonia increased, diarrhoea, hepatotoxicity, international normalised ratio increased, nausea, yellow skin, . REBIF dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient was hospitalized. Patient recovered.


Lactulose Side Effects Report #5628675-X
LACTULOSE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2008. Female patient, 43 years of age, weighting 185.0 lb, was diagnosed with hepatitis c and was treated with LACTULOSE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, amnesia, . LACTULOSE dosage: 30 ML Q DAU PO. Patient was hospitalized. Patient recovered.

Keppra Side Effects Report #5636471-2
Consumer or non-health professional from GERMANY reported KEPPRA problem on Feb 06, 2008. Female patient, 60 years of age, was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: ammonia increased, depressed level of consciousness, encephalopathy, . KEPPRA dosage: unknown. During the same period patient was treated with VALPROATE. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5638752-5
TACROLIMUS problem was reported by a Physician from JAPAN on Dec 05, 2007. Female patient, 66 years of age, weighting 108.0 lb, was diagnosed with rheumatoid arthritis and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: ammonia increased, beta-n-acetyl-d-glucosaminidase increased, condition aggravated, dyspnoea, hepatitis b, hepatorenal syndrome, lymphocyte count decreased, oedema, oedema peripheral, . TACROLIMUS dosage: 1.5 MG, UID/QD; ORAL, 3 MG, UID/QD; ORAL. During the same period patient was treated with PREDNONINE, METHOTREXATE, ENBREL, ETODOLAC, VOLTAREN, ISCOTIN. Patient died on 05/03/2007.

Keppra Side Effects Report #5641014-3
Consumer or non-health professional from GERMANY reported KEPPRA problem on Feb 12, 2008. Female patient was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: ammonia increased, depressed level of consciousness, psychotic disorder, . KEPPRA dosage: 1500 MG 3/D. During the same period patient was treated with VALPROATE. Patient recovered.

Valproate Side Effects Report #5645736-X
VALPROATE problem was reported by a Consumer or non-health professional from FRANCE on Feb 19, 2008. Male patient was diagnosed with epilepsy and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood lactate dehydrogenase abnormal, coagulation time prolonged, depressed level of consciousness, encephalopathy, hepatic failure, liver function test abnormal, vomiting, . VALPROATE dosage: INCREASING REGIMEN, MAXIMUM DAILY DOSE OF 25MG/KG). Patient was hospitalized. Patient recovered.


Keppra Side Effects Report #5648112-9
Consumer or non-health professional from GERMANY reported KEPPRA problem on Feb 15, 2008. Female patient, 60 years of age, was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: ammonia increased, depressed level of consciousness, disturbance in attention, . KEPPRA dosage: unknown. During the same period patient was treated with VALPROATE. Patient was hospitalized. Patient recovered.

Lantus Side Effects Report #5607518-4
LANTUS problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 21, 2008. Male patient, 56 years of age, was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: ammonia increased, . LANTUS dosage: unknown. During the same period patient was treated with OPTICLIK, FOLIC ACID, VITAMIN B 1, LACTULOSE, GLIPIZIDE, VITAMIN K, COMBIVENT. Patient was hospitalized. Patient recovered.

Lamictal Side Effects Report #5610708-8
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Jan 30, 2008. Male patient, weighting 165.0 lb, was diagnosed with bipolar i disorder and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, . LAMICTAL dosage: 25MG QDAY PO. During the same period patient was treated with VASOTEC, NEXIUM, CLARITIN, COMBIVENT, FLOVENT, COLACE, SENNA, RISPERDAL. Patient recovered.

Seroquel Side Effects Report #5542325-2
SEROQUEL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Male patient, 73 years of age, weighting 173.1 lb, was diagnosed with parkinson's disease and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood glucose increased, convulsion, dehydration, dementia, diabetic hyperosmolar coma, disorientation, hypernatraemia, lobar pneumonia, . SEROQUEL dosage: unknown. During the same period patient was treated with SYNTHROID, CARDIZEM, ARICEPT, SINEMET, LACTOSE, ASPIRIN, DILANTIN. Patient was hospitalized. Patient died on 02/26/2006.

Citalopram Side Effects Report #5550872-2
Health Professional from DENMARK reported CITALOPRAM HYDROBROMIDE problem on Jan 28, 2004. Male patient, weighting 8.16 lb, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, culture urine positive, escherichia infection, feeding disorder neonatal, maternal condition affecting foetus, protein urine present, . CITALOPRAM HYDROBROMIDE dosage: 10 MG QD TRANSPLACENTAL. During the same period patient was treated with CITALOPRAM HYDROBROMIDE. Patient was hospitalized. Patient recovered.


Revlimid Side Effects Report #5553429-2
REVLIMID problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 03, 2007. Male patient, 36 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood calcium increased, blood potassium increased, . REVLIMID dosage: 25 MG,1IN 1 D,ORAL. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5567733-5
Consumer or non-health professional from UNITED STATES reported NATALIZUMAB problem on Dec 05, 2007. Female patient, 39 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: ammonia increased, autoimmune disorder, immune system disorder, liver disorder, memory impairment, transient ischaemic attack, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with NEURONTIN, LYRICA, ZYRTEC, PROVIGIL, BACLOFEN, SKELAXIN. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5520673-X
EXJADE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 15, 2007. Male patient, 58 years of age, was diagnosed with iron metabolism disorder and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, coma, hepatic failure, . EXJADE dosage: 1750 MG, QD. Patient was hospitalized. Patient recovered.

Divalproex Side Effects Report #5526375-8
Pharmacist from UNITED STATES reported DIVALPROEX problem on Nov 21, 2007. Male patient, 56 years of age, was diagnosed with bipolar i disorder and was treated with DIVALPROEX. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, . DIVALPROEX dosage: 1000MG PM PO. Patient was hospitalized. Patient recovered.

Acetazolamide Side Effects Report #5528364-6
ACETAZOLAMIDE problem was reported by a Consumer or non-health professional from KOREA, REPUBLIC OF on Nov 20, 2007. Male patient, 49 years of age, was diagnosed with ataxia and was treated with ACETAZOLAMIDE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, ataxia, condition aggravated, dizziness, dysarthria, hyperammonaemia, metabolic acidosis, nystagmus, . ACETAZOLAMIDE dosage: 250MG, QID, ORAL. Patient was hospitalized. Patient recovered.

Rozerem Side Effects Report #5531916-0
Physician from UNITED STATES reported ROZEREM problem on Oct 10, 2007. Male patient, 50 years of age, was diagnosed with insomnia and was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: ammonia increased, hallucination, . ROZEREM dosage: unknown. Patient recovered.

Cymbalta Side Effects Report #5474652-1
CYMBALTA problem was reported by a Physician from UNITED STATES on Sept 18, 2007. Female patient was diagnosed with pain and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: ammonia increased, mood swings, vertebroplasty, . CYMBALTA dosage: 120 MG, DAILY (1/D). Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5477966-4
Physician from UNITED STATES reported NEXAVAR problem on Sept 28, 2007. Male patient, 75 years of age, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, pain in extremity, skin exfoliation, thrombocytopenia, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with LACTULOSE, PROTONIX, ALDACTONE, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Valproate Side Effects Report #5478679-5
VALPROATE problem was reported by a Health Professional from FRANCE on Sept 27, 2007. Male patient, 48 years of age, was diagnosed with epilepsy and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, cachexia, fatigue, food aversion, mobility decreased, somnolence, . VALPROATE dosage: unknown. During the same period patient was treated with TOPIRAMATE, CLONAZEPAM. Patient recovered.

Topiramate Side Effects Report #5487950-2
Pharmacist from UNITED STATES reported TOPIRAMATE problem on Oct 12, 2007. Male patient, 33 years of age, was diagnosed with bipolar i disorder and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, . TOPIRAMATE dosage: 25MG BID PO. Patient recovered.

Cefuroxime Side Effects Report #5491606-X
CEFUROXIME problem was reported by a Physician from UNITED STATES on Oct 19, 2007. Male patient, 52 years of age, was treated with CEFUROXIME. After drug was administered, patient experienced the following problems/side effects: ammonia increased, biopsy liver abnormal, confusional state, diabetes mellitus inadequate control, erythema, folliculitis, fungal infection, inflammation, liver injury, . CEFUROXIME dosage: unknown. During the same period patient was treated with NEURONTIN, INSULIN, ALBUTEROL, ADVAIR DISKUS, LISINOPRIL WITH HYDROCHLOROTHIAZIDE, FLEXERIL, ALLEGRO, CLARITIN. Patient recovered.

Avandamet Side Effects Report #5451423-3
Consumer or non-health professional from FRANCE reported AVANDAMET problem on Sept 04, 2007. Female patient, 67 years of age, was diagnosed with epilepsy and was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: ammonia increased, anorexia, aphasia, balance disorder, cognitive disorder, confusional state, metabolic encephalopathy, tremor, vomiting, . AVANDAMET dosage: unknown. During the same period patient was treated with TEGRETOL, DEPAKENE, NOVONORM, COTAREG, FENOFIBRATE, TENSTATEN, EQUANIL, VALIUM. Patient was hospitalized. Patient recovered.

Renagel Side Effects Report #5452123-6
RENAGEL problem was reported by a Pharmacist from UNITED STATES on Aug 30, 2007. Female patient, 50 years of age, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, . RENAGEL dosage: unknown. Patient was hospitalized. Patient recovered.

Risperdal Side Effects Report #5471102-6
Pharmacist from JAPAN reported RISPERDAL problem on Sept 20, 2007. Male patient, 52 years of age, was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood creatine phosphokinase increased, cirrhosis alcoholic, hyperglycaemia, . RISPERDAL dosage: unknown. During the same period patient was treated with FUROSEMIDE, LACTULOSE, HALOPERIDOL, ALDACTONE, ZOLPIDEM, LANSOPRAZOLE. Patient was hospitalized. Patient recovered.

Renagel Side Effects Report #5472145-9
RENAGEL problem was reported by a Pharmacist from UNITED STATES on Sept 12, 2007. Female patient, 50 years of age, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, . RENAGEL dosage: unknown. During the same period patient was treated with NIFEDIPINE, DIOVAN, SENSIPAR, GABAPENTIN, CLONIDINE, MINOXIDIL, LOMOTIL, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Ammonul Side Effects Report #5472548-2
Physician from FRANCE reported AMMONUL problem on Sept 11, 2007. Male patient was diagnosed with amino acid metabolism disorder and was treated with AMMONUL. After drug was administered, patient experienced the following problems/side effects: ammonia increased, disease progression, multi-organ failure, no therapeutic response, shock, . AMMONUL dosage: 5 ML/24 HOURS/IV. Patient died on 09/16/2007.

Depakote Side Effects Report #5486558-2
DEPAKOTE ER problem was reported by a Physician from UNITED STATES on Nov 02, 2006. Male patient, 45 years of age, was diagnosed with bipolar disorder and was treated with DEPAKOTE ER. After drug was administered, patient experienced the following problems/side effects: ammonia increased, toxic encephalopathy, . DEPAKOTE ER dosage: unknown. Patient was hospitalized. Patient recovered.

Depakote Side Effects Report #5486588-0
Consumer or non-health professional from UNITED STATES reported DEPAKOTE ER problem on Mar 07, 2007. Male patient, 72 years of age, was diagnosed with convulsion and was treated with DEPAKOTE ER. After drug was administered, patient experienced the following problems/side effects: ammonia increased, mental status changes, . DEPAKOTE ER dosage: 500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with LEVETIRACETAM. Patient was hospitalized. Patient recovered.

Pegasys Side Effects Report #5405097-8
PEGASYS problem was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2007. Male patient, 54 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: ammonia increased, cellulitis, full blood count decreased, hallucination, influenza like illness, psychotic disorder, renal failure, . PEGASYS dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5405661-6
Consumer or non-health professional from UNITED STATES reported EXJADE problem on Aug 02, 2007. Male patient, 58 years of age, was diagnosed with iron metabolism disorder and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, coma, hepatic failure, . EXJADE dosage: 1750 MG, QD. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5406889-1
NEXAVAR problem was reported by a Physician from UNITED STATES on July 31, 2007. Male patient, 75 years of age, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, thrombocytopenia, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with LACTULOSE, PROTONIX, ALDACTONE, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Vytorin Side Effects Report #5412935-1
Physician from UNITED STATES reported VYTORIN problem on Aug 09, 2007. Female patient, 68 years of age, was diagnosed with blood cholesterol increased and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: ammonia increased, disturbance in attention, hepatitis acute, loss of consciousness, pancreatitis acute, . VYTORIN dosage: unknown. During the same period patient was treated with THYROID. Patient was hospitalized and became disabled. Patient recovered.

Tacrolimus Side Effects Report #5427077-9
TACROLIMUS problem was reported by a Pharmacist from UNITED STATES on Aug 24, 2007. Male patient, weighting 235.0 lb, was diagnosed with immunosuppression and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: ammonia increased, hepatic cirrhosis, mental status changes, portal hypertension, . TACROLIMUS dosage: 2MG PO BID. During the same period patient was treated with REGULAR INSULIN, INSULIN ASPART, GLARGINE, ROSUVASTATIN, PREDNISONE, MYCOPHENOLATE MOFETIL, RANITIDINE, FISH OIL. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5379682-6
Physician from GERMANY reported SANDOSTATIN LAR problem on June 26, 2007. Female patient, 63 years of age, was diagnosed with neuroendocrine tumour and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, nausea, transaminases increased, . SANDOSTATIN LAR dosage: unknown. Patient was hospitalized. Patient recovered.

Pegasys Side Effects Report #5380460-2
PEGASYS problem was reported by a Consumer or non-health professional from UNITED STATES on June 25, 2007. Male patient, 50 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood magnesium decreased, blood potassium decreased, confusional state, depression, dysphonia, epistaxis, fatigue, haemoptysis, . PEGASYS dosage: STRENGTH REPORTED AS 180UG/0.5ML. During the same period patient was treated with RIBAVIRIN, ANTIDEPRESSANT NOS. Patient recovered.

Phenytoin Side Effects Report #5392144-5
Pharmacist from UNITED STATES reported PHENYTOIN problem on July 18, 2007. Male patient, 63 years of age, was diagnosed with convulsion and was treated with PHENYTOIN. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, hallucination, mental status changes, sedation, . PHENYTOIN dosage: 200MG BID PO. Patient was hospitalized. Patient recovered.

Topiramate Side Effects Report #5392534-0
TOPIRAMATE problem was reported by a Physician from RUSSIAN FEDERATION on July 09, 2007. Female patient, weighting 14.77 lb, was diagnosed with partial seizures and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, convulsion, enterocolitis, . TOPIRAMATE dosage: unknown. Patient was hospitalized. Patient recovered.

Depakote Side Effects Report #5394381-2
Physician from UNITED STATES reported DEPAKOTE problem on July 16, 2007. Male patient, weighting 156.1 lb, was diagnosed with convulsion, bicuspid aortic valve, asthma and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, dehydration, diarrhoea, gastroenteritis, influenza like illness, pneumonia, vomiting, . DEPAKOTE dosage: unknown. During the same period patient was treated with TOPIRAMATE, PRIMIDONE, METOPROLOL SUCCINATE, SINGULAIR, FLOVENT IH, ALBUTEROL IH. Patient was hospitalized. Patient recovered.

Valproic Side Effects Report #5397656-6
VALPROIC ACID problem was reported by a Pharmacist from UNITED STATES on July 23, 2007. Male patient, 24 years of age, weighting 179.0 lb, was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: ammonia increased, . VALPROIC ACID dosage: 1000 MG DAILY PO. Patient recovered.

Depakote Side Effects Report #5398174-1
Physician from UNITED STATES reported DEPAKOTE problem on July 16, 2007. Female patient, weighting 138.1 lb, was diagnosed with convulsion and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: ammonia increased, laboratory test abnormal, . DEPAKOTE dosage: unknown. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5379682-6
SANDOSTATIN LAR problem was reported by a Physician from GERMANY on June 26, 2007. Female patient, 63 years of age, was diagnosed with neuroendocrine tumour and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: ammonia increased, confusional state, nausea, transaminases increased, . SANDOSTATIN LAR dosage: unknown. Patient was hospitalized. Patient recovered.

Pegasys Side Effects Report #5380460-2
Consumer or non-health professional from UNITED STATES reported PEGASYS problem on June 25, 2007. Male patient, 50 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood magnesium decreased, blood potassium decreased, confusional state, depression, dysphonia, epistaxis, fatigue, haemoptysis, . PEGASYS dosage: STRENGTH REPORTED AS 180UG/0.5ML. During the same period patient was treated with RIBAVIRIN, ANTIDEPRESSANT NOS. Patient recovered.