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

ANOREXIA ( 10 FDA reports)
NEUTROPENIA ( 9 FDA reports)
PYREXIA ( 8 FDA reports)
DYSPNOEA ( 7 FDA reports)
PSORIASIS ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
INFUSION SITE OEDEMA ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
ANURIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SHOCK ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
FALL ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)

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