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

DEHYDRATION ( 7 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
PYREXIA ( 3 FDA reports)
THIRST ( 3 FDA reports)
RASH ( 3 FDA reports)
BLOOD URIC ACID DECREASED ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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