Please choose an event type to view the corresponding MedsFacts report:

COMPLETED SUICIDE ( 7 FDA reports)
RENAL FAILURE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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