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Emend Side Effects Report #5669356-6
Pharmacist from UNITED STATES reported EMEND problem on Mar 11, 2008. Male patient, 63 years of age, was diagnosed with prophylaxis of nausea and vomiting and was treated with EMEND. After drug was administered, patient experienced the following problems/side effects: asterixis, dyskinesia, muscular weakness, . EMEND dosage: unknown. During the same period patient was treated with MELPHALAN, ZOFRAN, DECADRON. Patient recovered.

Arava Side Effects Report #5580090-3
ARAVA problem was reported by a Physician from FRANCE on Dec 28, 2007. Female patient, 50 years of age, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bilirubin increased, encephalopathy, hepatitis fulminant, lupus hepatitis, transaminases increased, . ARAVA dosage: unknown. During the same period patient was treated with REMICADE, CORTANCYL. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5607850-4
Physician from FRANCE reported ARAVA problem on Jan 24, 2008. Female patient, 50 years of age, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bilirubin increased, encephalopathy, hepatitis fulminant, liver transplant, lupus hepatitis, post procedural complication, transaminases increased, . ARAVA dosage: unknown. During the same period patient was treated with REMICADE, CORTANCYL. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5568428-4
ARAVA problem was reported by a Physician from FRANCE on Dec 11, 2007. Female patient, 50 years of age, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bilirubin increased, encephalopathy, hepatitis fulminant, transaminases increased, . ARAVA dosage: unknown. During the same period patient was treated with REMICADE. Patient was hospitalized. Patient recovered.


Tegretol Side Effects Report #5572774-8
Consumer or non-health professional from JAPAN reported TEGRETOL problem on Dec 12, 2007. Female patient, 63 years of age, was diagnosed with epilepsy and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, dyskinesia, fall, gait disturbance, muscular weakness, . TEGRETOL dosage: 1200 MG/DAY. During the same period patient was treated with PHENYTOIN, ZONISAMIDE. Patient recovered.

Tegretol Side Effects Report #5572787-6
TEGRETOL problem was reported by a Consumer or non-health professional from JAPAN on Dec 13, 2007. Female patient, 44 years of age, was diagnosed with tonic convulsion and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, fall, muscular weakness, spinal compression fracture, . TEGRETOL dosage: unknown. During the same period patient was treated with VALPROATE, CLONAZEPAM, CLOBAZAM. Patient was hospitalized. Patient recovered.

Clozapine Side Effects Report #5576133-3
Physician from JAPAN reported CLOZAPINE problem on Dec 21, 2007. Female patient, 41 years of age, weighting 105.8 lb, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: asterixis, disease progression, disorientation, dysarthria, gait disturbance, hallucination, auditory, suicidal ideation, . CLOZAPINE dosage: unknown. During the same period patient was treated with LORAZEPAM, GLYSENNID, SELTOUCH. Patient was hospitalized. Patient recovered.

Clozapine Side Effects Report #5576601-4
CLOZAPINE problem was reported by a Physician from JAPAN on Dec 21, 2007. Female patient, 41 years of age, weighting 105.8 lb, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: asterixis, disease progression, disorientation, dysarthria, gait disturbance, hallucination, auditory, suicidal ideation, . CLOZAPINE dosage: unknown. During the same period patient was treated with LORAZEPAM, GLYSENNID, SELTOUCH. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5508675-0
Physician from FRANCE reported ARAVA problem on Oct 29, 2007. Female patient, 50 years of age, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bilirubin increased, encephalopathy, hepatitis fulminant, transaminases increased, . ARAVA dosage: unknown. During the same period patient was treated with REMICADE. Patient was hospitalized. Patient recovered.


Clozapine Side Effects Report #5474034-2
CLOZAPINE problem was reported by a Physician from JAPAN on Sept 18, 2007. Female patient, 41 years of age, weighting 105.8 lb, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: asterixis, disorientation, dysarthria, gait disturbance, . CLOZAPINE dosage: unknown. During the same period patient was treated with LORAZEPAM, PURSENNID, SELTOUCH. Patient was hospitalized. Patient recovered.

Clozapine Side Effects Report #5498535-6
Physician from JAPAN reported CLOZAPINE problem on Oct 15, 2007. Female patient, 41 years of age, weighting 105.8 lb, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: asterixis, disease progression, disorientation, dysarthria, gait disturbance, hallucination, auditory, suicidal ideation, . CLOZAPINE dosage: unknown. During the same period patient was treated with LORAZEPAM, GLYSENNID, SELTOUCH. Patient was hospitalized. Patient recovered.

Ciprofloxacin Side Effects Report #5451987-X
CIPROFLOXACIN problem was reported by a Physician from SAUDI ARABIA on Aug 31, 2007. Male patient, 46 years of age, was diagnosed with urinary tract infection pseudomonal and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: asterixis, asthenia, confusional state, disturbance in attention, metabolic encephalopathy, myoclonus, paraesthesia, somnolence, . CIPROFLOXACIN dosage: 250 MG, BID, ORAL. During the same period patient was treated with ACYCLOVIR. Patient was hospitalized. Patient recovered.

Ciprofloxacin Side Effects Report #5451989-3
Physician from SAUDI ARABIA reported CIPROFLOXACIN problem on Aug 31, 2007. Female patient, 67 years of age, was diagnosed with pneumonia and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: asterixis, confusional state, memory impairment, metabolic encephalopathy, myoclonus, somnolence, . CIPROFLOXACIN dosage: 200 MG, BID, INTRAVENOUS. During the same period patient was treated with CEFUROXIME, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5419427-4
ARIXTRA problem was reported by a Pharmacist from UNITED STATES on Aug 17, 2007. Female patient, 72 years of age, was diagnosed with atrial thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: asterixis, cardiac failure congestive, coagulopathy, dialysis, epistaxis, haematocrit decreased, renal failure, . ARIXTRA dosage: unknown. During the same period patient was treated with ALBUTEROL, ASPIRIN, QUESTRAN, PLAVIX, DIGOXIN, PROCRIT, LEXAPRO, LASIX. Patient was hospitalized. Patient died on 08/27/2006.


Lyrica Side Effects Report #5377769-5
Physician from GERMANY reported LYRICA problem on June 25, 2007. Female patient, weighting 233.7 lb, was diagnosed with intervertebral disc protrusion, spinal osteoarthritis and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: asterixis, . LYRICA dosage: unknown. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5377769-5
LYRICA problem was reported by a Physician from GERMANY on June 25, 2007. Female patient, weighting 233.7 lb, was diagnosed with intervertebral disc protrusion, spinal osteoarthritis and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: asterixis, . LYRICA dosage: unknown. Patient was hospitalized. Patient recovered.

Cefepime Side Effects Report #5773226-2
Pharmacist from UNITED STATES reported CEFEPIME problem on June 13, 2008. Male patient, 92 years of age, weighting 170.9 lb, was diagnosed with abdominal abscess and was treated with CEFEPIME. After drug was administered, patient experienced the following problems/side effects: asterixis, cardiac failure congestive, cardiopulmonary failure, hypoglycaemia, myoclonus, status epilepticus, toxic encephalopathy, . CEFEPIME dosage: unknown. During the same period patient was treated with FUROSEMIDE, ADVAIR DISKUS, METOPROLOL, ARANESP, HEPARIN, OMEPRAZOLE, VANCOMYCIN, AMOXICILLIN. Patient was hospitalized. Patient recovered.

Furosemide Side Effects Report #5739216-0
FUROSEMIDE problem was reported by a Consumer or non-health professional from FRANCE on May 13, 2008. Male patient, 61 years of age, was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bicarbonate increased, blood ph increased, depressed level of consciousness, diaphragmatic disorder, encephalopathy, hypercapnia, hypoventilation, lung infiltration, . FUROSEMIDE dosage: unknown. During the same period patient was treated with ESIDRIX, LASILIX, ZOCOR, NEO MERCAZOLE, XATRAL, TRIATEC, DIFFU K, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5740481-4
Physician from FRANCE reported NEXAVAR problem on Apr 01, 2008. Female patient, 68 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: asterixis, coma, convulsion, disease progression, extensor plantar response, hepatic encephalopathy, hepatic failure, lung disorder, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG. During the same period patient was treated with AUGMENTIN. Patient died on 02/25/2008.


Gabapentin Side Effects Report #5745820-6
GABAPENTIN problem was reported by a Physician from ITALY on May 08, 2008. Female patient, 76 years of age, was diagnosed with partial seizures and was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: asterixis, . GABAPENTIN dosage: 900 MG, QD; 300 MG, QD. During the same period patient was treated with OXCARBAZEPINE, LACIDIPINE, ACETYLSALICYLIC ACID. Patient was hospitalized and became disabled. Patient recovered.

Altace Side Effects Report #5747405-4
Consumer or non-health professional from FRANCE reported ALTACE problem on May 16, 2008. Female patient was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: asterixis, encephalopathy, hypercapnia, interstitial lung disease, mental disorder, metabolic acidosis, metabolic alkalosis, somnolence, . ALTACE dosage: 1.25 MG, QD. During the same period patient was treated with OFLOCET, LASILIX, FUROSEMIDE, ESIDRIX, ZOCOR, NEO MERCAZOLE, XATRAL, DIFFU K. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5690437-5
ARAVA problem was reported by a Consumer or non-health professional from MEXICO on Mar 24, 2008. Female patient, 42 years of age, weighting 147.7 lb, was diagnosed with psoriatic arthropathy, irritable bowel syndrome and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: asterixis, hepatotoxicity, ocular icterus, rash macular, . ARAVA dosage: unknown. During the same period patient was treated with METHOTREXATE, DICLOFENAC, ALPRAZOLAM, MESALAZINA. Patient recovered.

Arava Side Effects Report #5696176-9
Consumer or non-health professional from MEXICO reported ARAVA problem on Apr 01, 2008. Female patient, 42 years of age, weighting 147.7 lb, was diagnosed with irritable bowel syndrome and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: asterixis, hepatotoxicity, ocular icterus, rash macular, . ARAVA dosage: unknown. During the same period patient was treated with METHOTREXATE, DICLOFENAC, TAFIL, MESALAMINE. Patient recovered.

Esidrix Side Effects Report #5710926-4
ESIDRIX problem was reported by a Consumer or non-health professional from FRANCE on Apr 14, 2008. Male patient, 61 years of age, was treated with ESIDRIX. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bicarbonate increased, blood ph increased, depressed level of consciousness, diaphragmatic disorder, encephalopathy, hypercapnia, hypoventilation, lung infiltration, . ESIDRIX dosage: unknown. During the same period patient was treated with LASILIX, ZOCOR, NEO MERCAZOLE, XATRAL, TRIATEC, DIFFU K, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5719268-4
Consumer or non-health professional from GERMANY reported ACTOS problem on Apr 17, 2008. Male patient, 50 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: asterixis, atrial fibrillation, atrial flutter, cardiac failure, cyanosis, hypoxia, oedema peripheral, respiratory failure, skin ulcer, . ACTOS dosage: 45 MG PER ORAL; 30 MG (MG,) PER ORAL. During the same period patient was treated with COAPROVEL, METFORMIN, HYDROCHLOROTHIAZIDE, SERUMLIPIDREDUCING AGENTS, BETA BLOCKING AGENTS. Patient was hospitalized. Patient recovered.

Altace Side Effects Report #5723521-8
ALTACE problem was reported by a Consumer or non-health professional from FRANCE on Apr 21, 2008. Female patient was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: asterixis, encephalopathy, hypercapnia, interstitial lung disease, mental disorder, metabolic acidosis, metabolic alkalosis, somnolence, . ALTACE dosage: 1.25 MG, QD. During the same period patient was treated with OFLOCET, LASILIX, FUROSEMIDE, ESIDRIX, ZOCOR, NEO MERCAZOLE, XATRAL, DIFFU K. Patient was hospitalized. Patient recovered.

Galantamine Side Effects Report #5331015-7
Pharmacist from UNITED STATES reported GALANTAMINE HYDROBROMIDE problem on May 18, 2007. Male patient, 79 years of age, weighting 160.5 lb, was diagnosed with vascular dementia, vascular encephalopathy and was treated with GALANTAMINE HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: asterixis, dehydration, diarrhoea, dry mouth, dysarthria, eye disorder, facial palsy, hypoperfusion, miosis, . GALANTAMINE HYDROBROMIDE dosage: 16MG DAILY PO. During the same period patient was treated with GALANTAMINE HYDROBROMIDE, ALENDRONATE, CIPROFLOXACIN, CITALOPRAM HYDROBROMIDE, CLOPIDOGREL BISULPHATE, CYANOCOBALAMIN, DEPEND BOOST LINER, DEPEND UNDERGARMENT. Patient was hospitalized. Patient recovered.

Winrho Side Effects Report #5335544-1
WINRHO SDF problem was reported by a Physician from UNITED STATES on May 03, 2007. Male patient, 54 years of age, was diagnosed with idiopathic thrombocytopenic purpura and was treated with WINRHO SDF. After drug was administered, patient experienced the following problems/side effects: asterixis, cholangitis, cholestasis, chromaturia, coagulopathy, dyspnoea, fluid retention, graft versus host disease, haemangioma of skin, . WINRHO SDF dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.

Valtrex Side Effects Report #5303288-8
Pharmacist from JAPAN reported VALTREX problem on Apr 13, 2007. Male patient, 81 years of age, was diagnosed with herpes zoster, constipation, hypertension, pollakiuria and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: asterixis, blood calcium decreased, blood chloride decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood sodium decreased, blood urea increased, bradyphrenia, c-reactive protein increased, . VALTREX dosage: 1000MG TWICE PER DAY. During the same period patient was treated with MAGNESIUM OXIDE, CORINAEL. Patient was hospitalized. Patient recovered.

Omeprazole Side Effects Report #5309968-2
OMEPRAZOLE problem was reported by a Health Professional from FRANCE on Apr 19, 2007. Female patient, 52 years of age, weighting 94.80 lb, was diagnosed with arthralgia and was treated with OMEPRAZOLE. After drug was administered, patient experienced the following problems/side effects: asterixis, blood lactic acid increased, blood ph decreased, blood urea increased, coma, encephalopathy, grand mal convulsion, hyperglycaemia, . OMEPRAZOLE dosage: unknown. During the same period patient was treated with NEURONTIN, COLCHIMAX, TELZIR, NORVIR, EPIVIR, ZIAGEN, LASIX, CALCIDIA. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5311725-8
Pharmacist from UNITED STATES reported LYRICA problem on Apr 26, 2007. Female patient, 65 years of age, was diagnosed with neuropathy peripheral and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: asterixis, dyskinesia, tremor, . LYRICA dosage: 50 MG TWICE DAILY PO. During the same period patient was treated with REGULAR INSULIN, HYDRALAZINE, LISINOPRIL, CARVEDILOL, ESOMEPRAZOLE MAGNESIUM, POTASSIUM CHLORIDE, MONTELUKAST, ALPRAZOLAM. Patient was hospitalized. Patient recovered.

Amoxicillin Side Effects Report #5264842-5
AMOXICILLIN problem was reported by a Physician from FRANCE on Mar 13, 2007. Male patient, 68 years of age, weighting 138.9 lb, was diagnosed with dental disorder prophylaxis, gout and was treated with AMOXICILLIN. After drug was administered, patient experienced the following problems/side effects: asterixis, confusional state, depressed level of consciousness, encephalopathy, overdose, . AMOXICILLIN dosage: unknown. During the same period patient was treated with NEURONTIN, RENAGEL, ALLOPURINOL, KAYEXALATE, LANSOYL, CALCIUM. Patient was hospitalized. Patient recovered.

Depakote Side Effects Report #5272110-0
Pharmacist from UNITED STATES reported DEPAKOTE problem on Mar 20, 2007. Male patient, 55 years of age, weighting 207.0 lb, was diagnosed with bipolar disorder and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: asterixis, coordination abnormal, hepatic encephalopathy, myoclonus, . DEPAKOTE dosage: 500MG BID PO. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5639201-3
TEGRETOL problem was reported by a Consumer or non-health professional from JAPAN on Feb 19, 2008. Female patient, 63 years of age, weighting 94.80 lb, was diagnosed with epilepsy, hyperlipidaemia and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, bradycardia, dyskinesia, fall, gait disturbance, muscular weakness, osteomyelitis, . TEGRETOL dosage: 400 MG, TID. During the same period patient was treated with PHENYTOIN, ZONISAMIDE, LIPITOR. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5604747-0
Consumer or non-health professional from JAPAN reported TEGRETOL problem on Jan 22, 2008. Female patient, 63 years of age, weighting 94.80 lb, was diagnosed with epilepsy, hyperlipidaemia and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, bradycardia, dyskinesia, fall, gait disturbance, muscular weakness, osteomyelitis, . TEGRETOL dosage: 400 MG, TID. During the same period patient was treated with PHENYTOIN, ZONISAMIDE, LIPITOR. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5604758-5
TEGRETOL problem was reported by a Consumer or non-health professional from JAPAN on Jan 22, 2008. Female patient, 44 years of age, weighting 119.0 lb, was diagnosed with tonic convulsion, hypotension and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, dyskinesia, epilepsy, fall, muscular weakness, spinal compression fracture, . TEGRETOL dosage: unknown. During the same period patient was treated with SELENICA, CLONAZEPAM, MYSTAN AZWELL, METLIGINE. Patient was hospitalized. Patient recovered.

Clozapine Side Effects Report #5609270-5
Physician from JAPAN reported CLOZAPINE problem on Sept 18, 2007. Female patient, 41 years of age, weighting 105.8 lb, was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: anxiety, asterixis, disease progression, disorientation, dysarthria, gait disturbance, hallucination, auditory, suicidal ideation, . CLOZAPINE dosage: unknown. During the same period patient was treated with WYPAX, GLYSENNID, SELTOUCH. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5577803-3
TEGRETOL problem was reported by a Consumer or non-health professional from JAPAN on Dec 25, 2007. Female patient, 44 years of age, weighting 119.0 lb, was diagnosed with tonic convulsion, hypotension and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, dyskinesia, fall, muscular weakness, spinal compression fracture, . TEGRETOL dosage: unknown. During the same period patient was treated with SELENICA, RIVOTRIL, MYSTAN AZWELL, METLIGINE. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5577844-6
Consumer or non-health professional from JAPAN reported TEGRETOL problem on Dec 25, 2007. Female patient, 63 years of age, weighting 94.80 lb, was diagnosed with epilepsy, hyperlipidaemia and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: asterixis, dyskinesia, fall, gait disturbance, muscular weakness, . TEGRETOL dosage: 400 MG, TID. During the same period patient was treated with PHENYTOIN, ZONISAMIDE, LIPITOR. Patient recovered.

Prograf Side Effects Report #5484254-9
PROGRAF problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 28, 2007. Male patient, 50 years of age, was diagnosed with liver transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: anxiety, asterixis, blood creatine increased, blood culture positive, diarrhoea, enterococcal bacteraemia, enterococcal infection, hepatic encephalopathy, international normalised ratio increased, . PROGRAF dosage: 2 MG, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, URSODIOL, LEVOTHYROXINE, FLEXERIL, INTRON A, RIBAVIRIN, MIDODRINE HYDROCHLORIDE. Patient was hospitalized. Patient died on 01/03/2007.

Depakote Side Effects Report #5484420-2
Physician from FRANCE reported DEPAKOTE problem on Oct 04, 2007. Male patient, 56 years of age, was diagnosed with bipolar disorder and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: anxiety, asterixis, confusional state, disorientation, encephalopathy, extrapyramidal disorder, muscle rigidity, . DEPAKOTE dosage: unknown. During the same period patient was treated with TIANEPTINE, LITHIUM CARBONATE, LEVOTHYROXINE, AMISULPRIDE, TRIHEXYPHENIDYL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Valtrex Side Effects Report #5447492-7
VALTREX problem was reported by a Physician from JAPAN on Sept 04, 2007. Female patient, 90 years of age, weighting 92.59 lb, was diagnosed with herpes zoster, hypertension, insomnia and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, asterixis, cerebral atrophy, disorientation, dysarthria, ischaemia, nausea, renal failure acute, somnolence, . VALTREX dosage: unknown. During the same period patient was treated with VOLTAREN, CEFZON, MARZULENE, GENTACIN, ADALAT, CANDESARTAN CILEXETIL, PRAVASTATIN, ZOLPIDEM. Patient was hospitalized. Patient recovered.

Betaferon Side Effects Report #5409009-2
Physician from SPAIN reported BETAFERON problem on July 27, 2007. Female patient, 39 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETAFERON. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, asterixis, depressed level of consciousness, hepatic necrosis, liver transplant, . BETAFERON dosage: unknown. Patient recovered.

Keppra Side Effects Report #5413889-4
KEPPRA problem was reported by a Physician from FRANCE on July 25, 2007. Male patient, 34 years of age, weighting 145.1 lb, was diagnosed with epilepsy and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: anorexia, asterixis, asthenia, autoimmune thyroiditis, cholangitis sclerosing, cholestasis, diarrhoea, epilepsy, eye disorder, . KEPPRA dosage: 250 MG 2/D PO. During the same period patient was treated with EPITOMAX, GARDAN, SERESTA, DEPAKENE, URBANYL, VANCOMYCINE PCH, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5417791-3
Consumer or non-health professional from UNITED STATES reported PROGRAF problem on Aug 03, 2007. Male patient, 50 years of age, was diagnosed with liver transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: anxiety, asterixis, asthenia, bacteraemia, blood creatinine increased, diarrhoea, disease recurrence, enterococcal infection, epistaxis, . PROGRAF dosage: 3 MG, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, URSODIOL, LEVOTHYROXINE, FLEXERIL, INTRON A, RIBAVIRIN, MIDODRINE HYDROCHLORIDE. Patient was hospitalized. Patient died on 01/03/2007.

Betaseron Side Effects Report #5395566-1
BETASERON problem was reported by a Physician from SPAIN on July 12, 2007. Female patient, 39 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, asterixis, depressed level of consciousness, hepatic necrosis, . BETASERON dosage: unknown. Patient recovered.

Cefepime Side Effects Report #5401325-3
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported CEFEPIME problem on July 25, 2007. Female patient, 91 years of age, was diagnosed with urinary tract infection and was treated with CEFEPIME. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, asterixis, eye disorder, . CEFEPIME dosage: unknown. Patient recovered.

Betaseron Side Effects Report #5395566-1
BETASERON problem was reported by a Physician from SPAIN on July 12, 2007. Female patient, 39 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, asterixis, depressed level of consciousness, hepatic necrosis, . BETASERON dosage: unknown. Patient recovered.

Cefepime Side Effects Report #5401325-3
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported CEFEPIME problem on July 25, 2007. Female patient, 91 years of age, was diagnosed with urinary tract infection and was treated with CEFEPIME. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, asterixis, eye disorder, . CEFEPIME dosage: unknown. Patient recovered.

Prograf Side Effects Report #5705347-4
PROGRAF problem was reported by a Physician from JAPAN on Mar 25, 2008. Male patient, 58 years of age, weighting 147.7 lb, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, asterixis, dialysis, graft versus host disease, hepatic failure, hepatitis fulminant, pyrexia, renal impairment, . PROGRAF dosage: ORAL; 0.5 MG, BID, ORAL. During the same period patient was treated with PREDNISOLONE, MUCOSTA, LAC B, DEPAS, DIFLUCAN. Patient died on 10/24/2004.

Depakote Side Effects Report #5343119-3
Physician from FRANCE reported DEPAKOTE problem on May 24, 2007. Male patient, 56 years of age, was diagnosed with bipolar disorder and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: anxiety, asterixis, confusional state, disorientation, encephalopathy, extrapyramidal disorder, muscle rigidity, psychomotor skills impaired, . DEPAKOTE dosage: unknown. During the same period patient was treated with TIANEPTINE, LITHIUM CARBONATE, LEVOTHYROXINE, AMISULPRIDE, TRIHEXYPHENIDYL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.