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FEMUR FRACTURE ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
FALL ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COUGH ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
CHILLS ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)

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