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

DIARRHOEA ( 10 FDA reports)
TREMOR ( 7 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
HERPES ZOSTER OTICUS ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SCREAMING ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
CLONUS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CORECTOPIA ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYST ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SCAB ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIAPEDESIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGITIS ENTEROVIRAL ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
NASAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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