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

PYREXIA ( 6 FDA reports)
ANAEMIA ( 6 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
COUGH ( 5 FDA reports)
PNEUMONITIS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
VOMITING ( 3 FDA reports)
PURPURA ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NEUTRALISING ANTIBODIES ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
RASH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)

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