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

RASH ( 17 FDA reports)
DIARRHOEA ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
INTERSTITIAL LUNG DISEASE ( 15 FDA reports)
MALAISE ( 15 FDA reports)
LIVER DISORDER ( 14 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
APHTHOUS STOMATITIS ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FALL ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
COUGH ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
FEMUR FRACTURE ( 5 FDA reports)
ILEUS ( 5 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
THIRST ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANAL CANCER ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ERYTHEMA ELEVATUM DIUTINUM ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
PAIN ( 4 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 4 FDA reports)
PURPURA ( 4 FDA reports)
PYOTHORAX ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ZINC SULPHATE TURBIDITY INCREASED ( 4 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
MELANOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
REYE'S SYNDROME ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)

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