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HEADACHE ( 12 FDA reports)
APLASIA PURE RED CELL ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
DIZZINESS ( 10 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
FATIGUE ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
RECTAL POLYP ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
CONTUSION ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
FALL ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
POLYP ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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