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

ANAEMIA ( 15 FDA reports)
HOT FLUSH ( 7 FDA reports)
CONSTIPATION ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RASH ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PURPURA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
METASTASES TO STOMACH ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL NECROSIS ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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