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

PYREXIA ( 14 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
RASH ( 12 FDA reports)
TREMOR ( 10 FDA reports)
PNEUMONIA ( 9 FDA reports)
VOMITING ( 9 FDA reports)
DIARRHOEA ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
HEPATITIS B ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
ACNE ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
METASTATIC PAIN ( 5 FDA reports)
MYRINGITIS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 4 FDA reports)
URETERIC DILATATION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
JAUNDICE ACHOLURIC ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COUGH ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC OPERATION ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CATARACT ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PERICORONITIS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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