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

DRUG INTERACTION ( 10 FDA reports)
ENCEPHALITIS ( 8 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
LIGAMENT DISORDER ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
OSTEOTOMY ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
METASTATIC PAIN ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
SCRUB TYPHUS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
CATARACT ( 1 FDA reports)
DEATH ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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