ASTERIXIS side effect
What is ASTERIXIS ?Drugs associated with ASTERIXIS
AMARYL ARAVA ARIXTRA BETAFERON BETASERON CEFEPIME CIPROFLOXACIN CLOZAPINE COMBIPATCH DEPAKOTE EMEND FORTUM INTERFERON KEPPRA LACTULOSE LYRICA PROGRAF REBETOL TEGRETOL VALTREX VELCADEASTERIXIS : 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.
ASTERIXIS : Velcade Side Effects Report #5632685-6
VELCADE problem was reported by a Physician from UNITED STATES on Feb 07, 2008. Male patient was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: asterixis, muscular weakness, pyrexia, stem cell transplant, . VELCADE dosage: unknown. During the same period patient was treated with MELPHALAN, DEXAMETHASONE, NEURONTIN. Patient was hospitalized. Patient recovered.
ASTERIXIS : Arava Side Effects Report #5580090-3
Physician from FRANCE reported ARAVA problem 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.
ASTERIXIS : Arava Side Effects Report #5607850-4
ARAVA problem was reported by a Physician from FRANCE 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.
ASTERIXIS : Arava Side Effects Report #5568428-4
Physician from FRANCE reported ARAVA problem 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.
ASTERIXIS : Tegretol Side Effects Report #5572774-8
TEGRETOL problem was reported by a Consumer or non-health professional from JAPAN 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.
ASTERIXIS : Tegretol Side Effects Report #5572787-6
Consumer or non-health professional from JAPAN reported TEGRETOL problem 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.
ASTERIXIS : Amaryl Side Effects Report #5573185-1
AMARYL problem was reported by a Physician from JAPAN on Dec 17, 2007. Female patient was diagnosed with diabetes mellitus and was treated with AMARYL. After drug was administered, patient experienced the following problems/side effects: asterixis, . AMARYL dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : Amaryl Side Effects Report #5519295-6
AMARYL problem was reported by a Physician from JAPAN on Nov 13, 2007. Female patient was diagnosed with diabetes mellitus and was treated with AMARYL. After drug was administered, patient experienced the following problems/side effects: asterixis, . AMARYL dosage: unknown. Patient was hospitalized. Patient recovered.
ASTERIXIS : Clozapine Side Effects Report #5474034-2
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: asterixis, disorientation, dysarthria, gait disturbance, . CLOZAPINE dosage: unknown. During the same period patient was treated with LORAZEPAM, PURSENNID, SELTOUCH. Patient was hospitalized. Patient recovered.
ASTERIXIS : Clozapine Side Effects Report #5498535-6
CLOZAPINE problem was reported by a Physician from JAPAN 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.
ASTERIXIS : Ciprofloxacin Side Effects Report #5451987-X
Physician from SAUDI ARABIA reported CIPROFLOXACIN problem 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.
ASTERIXIS : Ciprofloxacin Side Effects Report #5451989-3
CIPROFLOXACIN problem was reported by a Physician from SAUDI ARABIA 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.
ASTERIXIS : Arixtra Side Effects Report #5419427-4
Pharmacist from UNITED STATES reported ARIXTRA problem 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : 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.
ASTERIXIS : Rebetol Side Effects Report #5570060-3
REBETOL problem was reported by a Physician from FRANCE on Dec 10, 2007. Male patient, 56 years of age, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: anaemia, anorexia, asterixis, blood creatinine increased, cardiac disorder, cerebellar atrophy, cerebral disorder, confusional state, disturbance in attention, . REBETOL dosage: 600 MG;QW; PO; 1200 MG;QW;PO; 200 MG;TIW; PO; 200 MG;BIW;PO. During the same period patient was treated with PEGASYS, KARDEGIC, TAREG, CELECTOL, CALTRATE. Patient was hospitalized. Patient recovered.
ASTERIXIS : Fortum Side Effects Report #5500843-7
Consumer or non-health professional from FRANCE reported FORTUM problem on Oct 22, 2007. Female patient, 35 years of age, was diagnosed with bronchopulmonary aspergillosis, epilepsy and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase abnormal, aspartate aminotransferase abnormal, asterixis, blood alkaline phosphatase abnormal, blood creatinine abnormal, blood urea abnormal, cholestasis, dyskinesia, encephalopathy, . FORTUM dosage: unknown. During the same period patient was treated with VFEND, NEURONTIN, VOLTAREN, KEPPRA, CIFLOX, IMOVANE, TERCIAN, SEVREDOL. Patient was hospitalized. Patient recovered.
ASTERIXIS : Lactulose Side Effects Report #5472289-1
LACTULOSE problem was reported by a Physician from UNITED STATES on Sept 17, 2007. Male patient, 57 years of age, was diagnosed with constipation and was treated with LACTULOSE. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain, asterixis, chronic hepatic failure, colonic atony, confusional state, constipation, encephalopathy, faecaloma, . LACTULOSE dosage: 30 ML, TID, ORAL, 45 ML, QID, 60 ML, QID, ORAL, DAILY ENEMAS WERE GIVEN, RECTAL. During the same period patient was treated with DULCOLAX, NEOMYCIN. Patient was hospitalized. Patient recovered.
ASTERIXIS : Interferon Side Effects Report #5417379-4
Health Professional from UNITED STATES reported INTERFERON ALFACON problem on Dec 11, 2006. Male patient, 72 years of age, weighting 133.0 lb, was diagnosed with hepatitis c and was treated with INTERFERON ALFACON. After drug was administered, patient experienced the following problems/side effects: abdominal distension, aortic calcification, asterixis, asthenia, bradycardia, cardiomegaly, chronic hepatic failure, chronic obstructive pulmonary disease, coma, . INTERFERON ALFACON dosage: unknown. During the same period patient was treated with ARANESP, SYNTHROID, CENTRUM, OSCAL, VITAMIN B, MAGNESIUM OXIDE, ZAROXOLYN, BICARBONATE. Patient was hospitalized. Patient recovered.
ASTERIXIS : Combipatch Side Effects Report #5398851-2
COMBIPATCH problem was reported by a Consumer or non-health professional from UNITED STATES on July 20, 2007. Female patient, 74 years of age, was diagnosed with menopausal symptoms, menopause, angina pectoris, hypertension, hypersensitivity and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arteriosclerosis coronary artery, asterixis, axillary mass, benign neoplasm of thyroid gland, breast cancer, breast cosmetic surgery, breast mass, breast pain, . COMBIPATCH dosage: unknown. During the same period patient was treated with ESTRATEST, PREMARIN, PROVERA, TOPROL, HYDROCHLORZIDE, NORVASC, PLAQUENIL, ALLEGRA. Patient recovered.
ASTERIXIS : Combipatch Side Effects Report #5398851-2
Consumer or non-health professional from UNITED STATES reported COMBIPATCH problem on July 20, 2007. Female patient, 74 years of age, was diagnosed with menopausal symptoms, menopause, angina pectoris, hypertension, hypersensitivity and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: abdominal pain, arteriosclerosis coronary artery, asterixis, axillary mass, benign neoplasm of thyroid gland, breast cancer, breast cosmetic surgery, breast mass, breast pain, . COMBIPATCH dosage: unknown. During the same period patient was treated with ESTRATEST, PREMARIN, PROVERA, TOPROL, HYDROCHLORZIDE, NORVASC, PLAQUENIL, ALLEGRA. Patient recovered.