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

PYREXIA ( 11 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
EXANTHEM ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
FALL ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
LIPID METABOLISM DISORDER ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
ALVEOLAR PROTEINOSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HERPETIC GINGIVOSTOMATITIS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TETANY ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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