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

PAIN IN EXTREMITY ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ANAEMIA POSTOPERATIVE ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
CALCIUM DEFICIENCY ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CONCUSSION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
FALL ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LOW TURNOVER OSTEOPATHY ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJURY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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