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

RENAL FAILURE ( 6 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NEUROTOXICITY ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEURALGIC AMYOTROPHY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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