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

DYSPNOEA ( 5 FDA reports)
RASH ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
COUGH ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
CONSTIPATION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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