ALTERED STATE OF CONSCIOUSNESS side effect
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Drugs associated with ALTERED STATE OF CONSCIOUSNESS
ABATACEPT ABILIFY ACETAMINOPHEN ACETYLSALICYLIC ACTONEL ACTOS ACYCLOVIR ADALAT ADVAIR ADVIL ALBENDAZOLE ALDACTONE ALEVE ALKERAN ALLEGRA ALLERGY ALPRAZOLAM ALTACE AMARYL AMBIEN AMEVIVE AMITIZA AMOXICILLIN ANAPEINEECTION ANTABUSE AREDIA ARICEPT ARIPIPRAZOLE ARIXTRA ARTIST ASPIRIN ATARAX AVELOX AVONEX BACLOFEN BETAFERON BETASERON BEVACIZUMAB BRIPLATIN BUPROPION BUSULFAN BUSULFEX CABASER CARBAMAZEPINE CARBOPLATINE CEFAZOLIN CEFEPIME CELECOX CELECOXIB CELESTAMINE CELEXA CETUXIMAB CHANTIX CIFLOX CIPROFLOXACIN CISPLATIN CITALOPRAM CLAMOXYL CLARITIN CLOFARABINE CLOZAPINE CONCERTA COUMADIN CRAVIT CRESTOR CYCLOPHOSPHAMIDE CYCLOSPORINE CYMBALTA DACOGEN DALTEPARIN DECADRON DECITABINE DEFINITY DENOSINE DEPAKENE DEROXAT DESFERAL DEXTROMETHORPHAN DICLOFENAC DIGOXIN DILATREND DIOVAN DIPRIVAN DOCETAXEL DORNER DUROTEP EFFEXOR ELSPAR ENBREL ENDOXAN EPHEDRINE EPIRUBICIN EPLERENONE EPTIFIBATIDE ERBITUX ETOPOSIDE FABRAZYME FENTANYL FLAGYL FLUOXETINE FORTEO FORTUM FOZITEC FRESH FUROSEMIDE GABAPEN GABAPENTIN GAMMAGARD GATIFLO GEMZAR GLEEVEC GLIVEC GLUCOBAY HALCION HALDOL HUMIRA HYZAAR IFOMIDE IMMUCYST IMODIUM IMURAN INDAPAMIDE INFED IRESSA IRINOTECAN IZILOX JZOLOFT KALETRA KEPPRA LAMICTAL LAMOTRIGINE LANSOPRAZOLE LANTUS LAPATINIB LARIAM LASIX LEVAQUIN LINEZOLID LIORESAL LIPITOR LISPRO LITHIUM LORAZEPAM LOSARTAN LOXONIN LUCENTIS LUNESTA LUVOX LYRICA MAXALT MECTIZAN MEMANTINE METFORMIN METHOTREXATE METHOXY METOCLOPRAMIDE METOPROLOL MICARDIS MIDODRINE MIGLITOLLET MIRTAZAPINE MORPHINE MUCINEX MYCOPHENOLATE MYFORTIC NATALIZUMAB NATEGLINIDE NEORAL NEXIUM NIMOTOP NISIS NORITREN NORVASC NORVIR NOVOLOG NOVORAPID NOXAFIL OLANZAPINE OLMETEC OMEPRAL OMNISCAN OPANA OXYCODONE PARAPLATIN PARNATE PAROXETINE PAXIL PEGASYS PEMETREXED PEPCID PERIDONTIL PERMAX PRAMIPEXOLE PRAZOSIN PREZISTA PRIMAXIN PROGRAF PROPOFOL PROZAC QUETIAPINE QUIBRON RALOXIFENE RASILEZ REGULAR RELENZA REMICADE REQUIP RESLIN RIBAVIRIN RILUZOLE RINDERON RISPERDAL RITALIN RITUXAN RIVOTRIL ROCEPHIN SALAZOPYRIN SERETIDE SEROQUEL SEROXAT SOLANAX STRATTERA STROMECTOL SUBOXONE SUPRANE SUTENT TACROLIMUS TAKEPRON TAMIFLU TAMOXIFEN TARKA TAXOL TAXOTERE TEGRETOL TEMESTA TEMODAL TEMOZOLOMIDE THEOPHYLLINE TICLOPIDINE TIZANIDINE TOPALGIC TOPROL TRACLEER TRAMADOL TRASTUZUMAB TRISENOX TYSABRI VALACYCLOVIR VALTREX VECURONIUM VELCADE VERAPAMIL VESICARE VFEND VIAGRA VIREAD VISIPAQUE VOLTAREN WARFARIN XELODA XUSAL XYLOCAINE XYZAL ZANTAC ZELITREX ZETIA ZIAGEN ZINNAT ZITHROMAX ZOFRAN ZOLEDRONATE ZOLOFT ZOLPIDEM ZOMETA ZOMIG ZOVIRAX ZYPREXADiprivan Side Effects Report #5646840-2
Physician from JAPAN reported DIPRIVAN problem on Feb 27, 2008. Male patient, 38 years of age, weighting 286.6 lb, was diagnosed with sedation and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . DIPRIVAN dosage: unknown. Patient recovered.
Valtrex Side Effects Report #5646982-1
VALTREX problem was reported by a Pharmacist from JAPAN on Feb 26, 2008. Female patient, 89 years of age, weighting 103.6 lb, was diagnosed with herpes virus infection, hypertension, diabetes mellitus, cerebral infarction, nerve injury, osteoporosis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, dysarthria, gait disturbance, renal failure acute, speech disorder, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with BLOPRESS, TORSEMIDE, GLYBURIDE, ASPIRIN, MECOBALAMIN, RISEDRONATE. Patient was hospitalized. Patient recovered.
Lamictal Side Effects Report #5646999-7
Pharmacist from FRANCE reported LAMICTAL problem on Feb 29, 2008. Female patient, 74 years of age, weighting 220.5 lb, was diagnosed with convulsion, rheumatoid arthritis and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, cholestasis, confusional state, fatigue, hepatic encephalopathy, hepatic enzyme increased, hepatitis fulminant, prothrombin time prolonged, . LAMICTAL dosage: unknown. During the same period patient was treated with NOVATREX, CORTANCYL, GARDENAL, TRIVASTAL. Patient was hospitalized. Patient died on 01/30/2008.
Valtrex Side Effects Report #5648680-7
VALTREX problem was reported by a Pharmacist from JAPAN on Feb 29, 2008. Female patient, 89 years of age, weighting 103.6 lb, was diagnosed with herpes virus infection, hypertension, diabetes mellitus, cerebral infarction, nerve injury, osteoporosis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, dysarthria, gait disturbance, renal failure acute, speech disorder, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with BLOPRESS, TORSEMIDE, GLYBURIDE, ASPIRIN, MECOBALAMIN, RISEDRONATE. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5648686-8
Physician from JAPAN reported VALTREX problem on Feb 26, 2008. Female patient, 88 years of age, weighting 101.4 lb, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, delirium, dysarthria, renal impairment, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with DEPAS, LOXONIN, SELBEX, AMLODIN. Patient was hospitalized. Patient recovered.
Diprivan Side Effects Report #5648812-0
DIPRIVAN problem was reported by a Physician from JAPAN on Feb 28, 2008. Male patient, 75 years of age, weighting 121.3 lb, was diagnosed with sedation and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, anuria, . DIPRIVAN dosage: unknown. During the same period patient was treated with DOPAMINE, RADICUT. Patient recovered.
Primaxin Side Effects Report #5649000-4
Physician from JAPAN reported PRIMAXIN problem on Feb 27, 2008. Female patient, 63 years of age, was diagnosed with pneumonia and was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, condition aggravated, epilepsy, hyponatraemia, neuroleptic malignant syndrome, respiratory disorder, schizophrenia, . PRIMAXIN dosage: unknown. Patient recovered.
Micardis Side Effects Report #5649721-3
MICARDIS problem was reported by a Physician from JAPAN on Feb 28, 2008. Female patient, weighting 104.7 lb, was diagnosed with hypertension and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, hypoglycaemia, . MICARDIS dosage: unknown. During the same period patient was treated with AMLODIN, ALOSEN, FAMOTIDINE, FRANDOL, LASIX. Patient was hospitalized and became disabled. Patient recovered.
Visipaque Side Effects Report #5650590-6
Pharmacist from UNITED STATES reported VISIPAQUE problem on Mar 04, 2008. Female patient, weighting 176.4 lb, was diagnosed with catheterisation cardiac and was treated with VISIPAQUE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, aphasia, apnoea, blood pressure increased, corneal reflex decreased, hemiparesis, nih stroke scale score increased, no therapeutic response, . VISIPAQUE dosage: 175ML ONCE IV. Patient was hospitalized. Patient recovered.
Advair Side Effects Report #5651010-8
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 29, 2008. Female patient, 56 years of age, weighting 127.2 lb, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, bradycardia, bronchospasm, cardio-respiratory arrest, cardiogenic shock, coronary artery disease, dyspnoea, mitral valve incompetence, myocardial infarction, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with PACEMAKER PLACEMENT, LEVOPHED, ATROVENT, NYSTATIN, XOPENEX, ROBITUSSIN, RESTORIL, HEPARIN. Patient died on 12/19/2005.
Valtrex Side Effects Report #5651057-1
Physician from JAPAN reported VALTREX problem on Feb 27, 2008. Female patient, 87 years of age, weighting 83.78 lb, was diagnosed with herpes zoster, atrial fibrillation and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, dizziness, dysarthria, motor dysfunction, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with BEPRICOR, TAKEPRON, SELOKEN, CALTAN, ASPIRIN. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5653432-8
VALTREX problem was reported by a Physician from JAPAN on Feb 29, 2008. Female patient, 82 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, depressed level of consciousness, renal failure acute, somnolence, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with NORVASC, BLOPRESS, ANPLAG, SELBEX, TRICOR, DEPAS, TRIAZOLAM, KINEDAK. Patient was hospitalized. Patient recovered.
Reslin Side Effects Report #5653630-3
Physician from JAPAN reported RESLIN problem on Feb 18, 2008. Female patient, 70 years of age, was diagnosed with delirium, insomnia and was treated with RESLIN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, delirium, . RESLIN dosage: unknown. During the same period patient was treated with MYSLEE. Patient was hospitalized. Patient recovered.
Primaxin Side Effects Report #5655382-X
PRIMAXIN problem was reported by a Physician from JAPAN on Feb 27, 2008. Male patient, 55 years of age, was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, arrhythmia, . PRIMAXIN dosage: unknown. Patient died on 02/20/2008.
Valtrex Side Effects Report #5656971-9
Physician from JAPAN reported VALTREX problem on Mar 06, 2008. Female patient, 85 years of age, weighting 97.00 lb, was diagnosed with herpes zoster, depression, constipation, gastric ulcer, hypertension, polyuria, vomiting and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, asthenia, blood creatinine increased, blood potassium increased, blood urea increased, dehydration, eating disorder, hyperkalaemia, hypokinesia, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with SERMION, TOLEDOMIN, MAGLAX, TOWARAT L, SPIRONOLACTONE. Patient was hospitalized. Patient died on 12/31/2007.
Diprivan Side Effects Report #5657020-9
DIPRIVAN problem was reported by a Physician from JAPAN on Mar 05, 2008. Male patient, 38 years of age, weighting 286.6 lb, was diagnosed with sedation and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . DIPRIVAN dosage: unknown. Patient recovered.
Irinotecan Side Effects Report #5657376-7
Health Professional from JAPAN reported IRINOTECAN problem on Feb 27, 2008. Female patient, 73 years of age, weighting 116.8 lb, was diagnosed with gastric cancer, nutritional support and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, diarrhoea, leukopenia, neutropenia, thrombocytopenia, . IRINOTECAN dosage: unknown. During the same period patient was treated with CISPLATIN, DECADRON, NASEA, PRIMPERAN, FULCALIQ. Patient was hospitalized. Patient died on 06/18/2007.
Vecuronium Side Effects Report #5657954-5
VECURONIUM BROMIDE problem was reported by a Consumer or non-health professional from JAPAN on Feb 22, 2008. Male patient, 59 years of age, was treated with VECURONIUM BROMIDE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . VECURONIUM BROMIDE dosage: 1 MG Q1HR. Patient was hospitalized. Patient recovered.
Loxonin Side Effects Report #5659541-1
Consumer or non-health professional from JAPAN reported LOXONIN problem on Mar 06, 2008. Male patient, 73 years of age, weighting 147.7 lb, was diagnosed with pain, abdominal discomfort, constipation, prostate cancer, hypertension, metastases to bone and was treated with LOXONIN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, c-reactive protein increased, disseminated intravascular coagulation, gamma-glutamyltransferase increased, . LOXONIN dosage: 120 MG. During the same period patient was treated with TAKEPRON, MAGMITT, ALOSENN, VOLTAREN, CODEINE PHOSPHATE, CASODEX, AMLODIN, ZOMETA. Patient was hospitalized. Patient recovered.
Theophylline Side Effects Report #5660588-X
THEOPHYLLINE problem was reported by a Physician from JAPAN on Feb 29, 2008. Female patient, 61 years of age, was diagnosed with asthma, neuralgia, cancer pain, constipation, angina pectoris, gastric ulcer, depression and was treated with THEOPHYLLINE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood creatine phosphokinase increased, blood pressure decreased, convulsion, tachycardia, . THEOPHYLLINE dosage: 200 MG, DAILY. During the same period patient was treated with AMOXAPINE, OXYCODONE, FENTANYL, SENNOSIDES, NICORANDIL, FAMOTIDINE, FLUVOXAMINE MALEATE, LITHIUM CARBONATE. Patient was hospitalized. Patient recovered.
Toprol Side Effects Report #5660904-9
Consumer or non-health professional from UNITED STATES reported TOPROL problem on Mar 04, 2008. Female patient, 80 years of age, was diagnosed with urinary tract infection and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . TOPROL dosage: unknown. During the same period patient was treated with LEVAQUIN, PREDNISONE, NORVASC. Patient recovered.
Requip Side Effects Report #5661725-3
REQUIP problem was reported by a Physician from JAPAN on Mar 10, 2008. Male patient, 59 years of age, was diagnosed with parkinson's disease and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, somnolence, sudden onset of sleep, . REQUIP dosage: 6MG THREE TIMES PER DAY. During the same period patient was treated with CARBIDOPA AND LEVODOPA, POLLAKISU, COMTAN. Patient was hospitalized. Patient recovered.
Keppra Side Effects Report #5661757-5
Consumer or non-health professional from GERMANY reported KEPPRA problem on Feb 20, 2008. Female patient, 71 years of age, weighting 132.3 lb, was diagnosed with epilepsy, depression and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, hyponatraemia, unresponsive to stimuli, . KEPPRA dosage: 1000 MG 2/D. During the same period patient was treated with MIRTAZAPINE. Patient was hospitalized. Patient recovered.
Rituxan Side Effects Report #5662807-2
RITUXAN problem was reported by a Physician from JAPAN on Mar 05, 2008. Female patient, weighting 103.6 lb, was diagnosed with non-hodgkin's lymphoma, pruritus, urticaria and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . RITUXAN dosage: 375 MG/M2, QD. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, MEQUITAZINE, HYDROCORTISONE, CHLORIDE, CHLORIDE. Patient recovered.
Valtrex Side Effects Report #5663114-4
Physician from JAPAN reported VALTREX problem on Mar 10, 2008. Male patient, 75 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, convulsion, dyskinesia, . VALTREX dosage: 1000MG THREE TIMES PER DAY. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5663115-6
VALTREX problem was reported by a Physician from JAPAN on Mar 10, 2008. Male patient, 75 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, convulsion, dyskinesia, . VALTREX dosage: unknown. During the same period patient was treated with ZOVIRAX. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5663133-8
Physician from JAPAN reported VALTREX problem on Mar 11, 2008. Female patient, 70 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, dizziness, fear, hallucination, motor dysfunction, nervous system disorder, . VALTREX dosage: 1000MG PER DAY. During the same period patient was treated with LOXONIN. Patient recovered.
Vecuronium Side Effects Report #5663312-X
VECURONIUM BROMIDE problem was reported by a Consumer or non-health professional from JAPAN on Mar 03, 2008. Male patient, 59 years of age, was treated with VECURONIUM BROMIDE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . VECURONIUM BROMIDE dosage: 1 MG Q1HR. During the same period patient was treated with PROPOFOL. Patient was hospitalized. Patient died.
Tacrolimus Side Effects Report #5663440-9
Physician from JAPAN reported TACROLIMUS problem on Feb 21, 2008. Female patient, 33 years of age, was diagnosed with lupus nephritis and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . TACROLIMUS dosage: 2 MG, D, ORAL. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5663527-0
VELCADE problem was reported by a Physician from JAPAN on Feb 22, 2008. Male patient, 74 years of age, weighting 101.4 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, constipation, diarrhoea, disease progression, hypoaesthesia, nausea, pneumonia aspiration, renal impairment, thrombocytopenia, . VELCADE dosage: 1.80 MG, INTRAVENOUS; 1.40 MG, INTRAVENOUS; 1.00 MG, INTRAVENOUS. During the same period patient was treated with HYDROCORTISONE SUCCINATE, NIFEDIPINE, PROTECADIN, ALLOPURINOL, BICARBONATE, SOLITA T. Patient was hospitalized. Patient died on 10/23/2007.
Decitabine Side Effects Report #5663709-8
Health Professional from SPAIN reported DECITABINE problem on Feb 27, 2008. Male patient, 73 years of age, was diagnosed with acute myeloid leukaemia and was treated with DECITABINE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, cardiomegaly, cardiopulmonary failure, cholestasis, confusional state, disorientation, epistaxis, . DECITABINE dosage: 36 MG, INTRAVENOUS. During the same period patient was treated with MEROPENEM, ONDANSETRON, FUROSEMIDA, TEICOPLANINA, AMIKACINA. Patient was hospitalized. Patient died on 03/26/2007.
Arixtra Side Effects Report #5664481-8
ARIXTRA problem was reported by a Physician from FRANCE on Mar 07, 2008. Female patient, 73 years of age, weighting 172.0 lb, was diagnosed with pulmonary embolism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, arthralgia, brain herniation, cerebral haematoma, cerebral haemorrhage, joint swelling, mydriasis, vomiting, . ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient died on 10/23/2007.
Irinotecan Side Effects Report #5664870-1
Health Professional from JAPAN reported IRINOTECAN problem on Mar 04, 2008. Female patient, weighting 116.8 lb, was diagnosed with gastric cancer, brain oedema, nutritional support and was treated with IRINOTECAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, anorexia, diarrhoea, dysphagia, leukopenia, nausea, neutropenia, thrombocytopenia, vomiting, . IRINOTECAN dosage: DAILY DOSE:100MG. During the same period patient was treated with CISPLATIN, DECADRON, NASEA, PRIMPERAN, FULCALIQ. Patient was hospitalized. Patient died on 06/18/2007.
Celecox Side Effects Report #5665153-6
CELECOX problem was reported by a Physician from JAPAN on Mar 04, 2008. Female patient, 71 years of age, was diagnosed with back pain and was treated with CELECOX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, headache, nausea, pyrexia, vomiting, . CELECOX dosage: unknown. Patient was hospitalized. Patient recovered.
Aricept Side Effects Report #5668679-4
Physician from JAPAN reported ARICEPT problem on Mar 06, 2008. Male patient, 74 years of age, weighting 112.4 lb, was diagnosed with dementia alzheimer's type and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood chloride increased, blood magnesium increased, blood sodium increased, haemodialysis, renal failure acute, . ARICEPT dosage: 5 MG, 1 IN 1 D, ORAL. During the same period patient was treated with HALOPERIDOL, ASPIRIN, ALLOPURINOL, KNORAMIN, UBRETID, MARILEON, MAGMITT, URSO. Patient was hospitalized. Patient recovered.
Neoral Side Effects Report #5670109-3
NEORAL problem was reported by a Physician from JAPAN on Mar 05, 2008. Male patient, 44 years of age, was diagnosed with renal transplant and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, anaemia, back pain, computerised tomogram abnormal, continuous haemodiafiltration, cytomegalovirus infection, diabetes mellitus, hepatic function abnormal, hyperlipidaemia, . NEORAL dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE, CELLCEPT. Patient was hospitalized. Patient recovered.
Dalteparin Side Effects Report #5670195-0
Physician from CZECH REPUBLIC reported DALTEPARIN problem on Feb 29, 2008. Female patient, 24 years of age, was diagnosed with cerebral venous thrombosis and was treated with DALTEPARIN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, cerebral venous thrombosis, condition aggravated, intracranial venous sinus thrombosis, transverse sinus thrombosis, . DALTEPARIN dosage: unknown. During the same period patient was treated with PROGESTERONE, ANTIBIOTICS. Patient was hospitalized. Patient recovered.
Deroxat Side Effects Report #5670926-X
DEROXAT problem was reported by a Pharmacist from FRANCE on Mar 07, 2008. Female patient was treated with DEROXAT. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, intentional overdose, suicide attempt, . DEROXAT dosage: 280MG SINGLE DOSE. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5671363-4
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Mar 06, 2008. Female patient, weighting 175.0 lb, was diagnosed with depression and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, anger, anxiety, emotional disorder, fear, feeling abnormal, flight of ideas, irritability, malaise, . CHANTIX dosage: unknown. During the same period patient was treated with SEROQUEL, CLONAZEPAM, EFFEXOR, AMBIEN, GEODON. Patient recovered.
Depakene Side Effects Report #5672587-2
DEPAKENE problem was reported by a Physician from JAPAN on Mar 10, 2008. Female patient, 27 years of age, weighting 156.5 lb, was diagnosed with partial seizures and was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, dizziness, eye movement disorder, feeling drunk, nausea, oral intake reduced, somnolence, . DEPAKENE dosage: 200 MG. During the same period patient was treated with NITRAZEPAM, TEGRETOL. Patient was hospitalized. Patient recovered.
Imuran Side Effects Report #5672955-9
Physician from JAPAN reported IMURAN problem on Mar 13, 2008. Female patient, 24 years of age, was treated with IMURAN. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, convulsion, cyst, cytomegalovirus viraemia, hyperglycaemia, lymphoma, pleural effusion, pneumonia staphylococcal, pneumothorax, . IMURAN dosage: 100MG PER DAY. During the same period patient was treated with PROGRAF, FENTANEST, FUNGIZONE, DIPRIVAN, ROPIVACAINE, VANCOMYCIN, MYSLEE. Patient was hospitalized. Patient recovered.
Hyzaar Side Effects Report #5673725-8
HYZAAR problem was reported by a Physician from JAPAN on Mar 12, 2008. Male patient, 77 years of age, was diagnosed with hypertension and was treated with HYZAAR. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, . HYZAAR dosage: unknown. During the same period patient was treated with NORVASC. Patient recovered.
Luvox Side Effects Report #5673970-1
Consumer or non-health professional from JAPAN reported LUVOX problem on Mar 01, 2008. Male patient, 57 years of age, was diagnosed with depression, anxiety, tremor and was treated with LUVOX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, apathy, electroencephalogram abnormal, memory impairment, . LUVOX dosage: (150 MG, 1 D), ORAL. During the same period patient was treated with PAROXETINE, CLOXAZOLAM, FLUPHENAZINE, TRIHEXYPHENIDYL, ZOLPIDEM TARTRATE. Patient recovered.
Amitiza Side Effects Report #5674600-5
AMITIZA problem was reported by a Pharmacist from UNITED STATES on Mar 19, 2008. Female patient, 24 years of age, weighting 130.0 lb, was diagnosed with irritable bowel syndrome and was treated with AMITIZA. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, chest pain, dizziness, hypoaesthesia, musculoskeletal pain, nausea, pain in extremity, tachycardia, . AMITIZA dosage: unknown. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5674688-1
Physician from JAPAN reported VALTREX problem on Mar 17, 2008. Female patient, 82 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, depressed level of consciousness, renal failure acute, somnolence, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with NORVASC, BLOPRESS, ANPLAG, SELBEX, TRICOR, DEPAS, TRIAZOLAM, KINEDAK. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5675902-9
VALTREX problem was reported by a Physician from JAPAN on Mar 18, 2008. Male patient, 75 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, convulsion, diplopia, dyskinesia, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with ZOVIRAX, CYANOCOBALAMIN, SIGMART, FUROSEMIDE, SELOKEN, TAKEPRON, ALLELOCK, CALTAN. Patient was hospitalized. Patient recovered.
Paxil Side Effects Report #5675921-2
Pharmacist from JAPAN reported PAXIL problem on Mar 18, 2008. Male patient, 37 years of age, was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, overdose, . PAXIL dosage: unknown. During the same period patient was treated with LENDORMIN. Patient was hospitalized. Patient recovered.
Aldactone Side Effects Report #5676433-2
ALDACTONE problem was reported by a Consumer or non-health professional from JAPAN on Mar 14, 2008. Male patient, 28 years of age, was treated with ALDACTONE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, anuria, intentional overdose, suicide attempt, . ALDACTONE dosage: unknown. Patient recovered.
Aricept Side Effects Report #5676636-7
Physician from JAPAN reported ARICEPT problem on Mar 12, 2008. Female patient, 85 years of age, was diagnosed with dementia and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, bradycardia, convulsion, hepatic function abnormal, hypotension, thrombocytopenia, . ARICEPT dosage: 3 MG, 1 IN 1 D, ORAL. During the same period patient was treated with TETRAMIDE, DOGMATYL. Patient was hospitalized. Patient recovered.
Aricept Side Effects Report #5676656-2
ARICEPT problem was reported by a Physician from JAPAN on Mar 11, 2008. Female patient, 78 years of age, was diagnosed with dementia alzheimer's type, bipolar i disorder, hypertension and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood pressure decreased, hyperhidrosis, myoclonus, pyrexia, sinus bradycardia, urine output decreased, . ARICEPT dosage: 3 MG, 1 IN 1 D, ORAL; 5 MG, 1 IN D, ORAL. During the same period patient was treated with LITHIUM CARBONATE, NORVASC, DIOVAN, SEIBULE, PRAVASTATIN. Patient recovered.
Aricept Side Effects Report #5676663-X
Physician from JAPAN reported ARICEPT problem on Mar 07, 2008. Female patient, 51 years of age, weighting 82.67 lb, was diagnosed with dementia, depression and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood pressure systolic decreased, body temperature increased, cardiac arrest, coma, continuous haemodiafiltration, dehydration, dementia alzheimer's type, dialysis, . ARICEPT dosage: 5 MG, 1 IN 1 D, ORAL. During the same period patient was treated with TOLEDOMIN, TETRAMIDE, DORAL, MAGLAX, MEILAX, HALCION. Patient died on 01/30/2008.