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

DRUG INEFFECTIVE ( 5 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTROINTESTINAL PAIN ( 4 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
DEATH ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
ABASIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)

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