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

LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
GASTRIC POLYPS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
LEUKOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CACHEXIA ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
URINE SODIUM DECREASED ( 2 FDA reports)
URINE CHLORIDE DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)

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