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

PAIN ( 35 FDA reports)
ABDOMINAL PAIN UPPER ( 26 FDA reports)
DYSPNOEA ( 26 FDA reports)
INJURY ( 25 FDA reports)
HYPOAESTHESIA ( 23 FDA reports)
WEIGHT DECREASED ( 23 FDA reports)
PALPITATIONS ( 22 FDA reports)
MIGRAINE ( 21 FDA reports)
ANXIETY ( 20 FDA reports)
CEREBROVASCULAR ACCIDENT ( 20 FDA reports)
NAUSEA ( 20 FDA reports)
ANHEDONIA ( 19 FDA reports)
BACK PAIN ( 19 FDA reports)
DEPRESSION ( 19 FDA reports)
FALL ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 18 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 18 FDA reports)
VISION BLURRED ( 18 FDA reports)
AGITATION ( 17 FDA reports)
ANKLE FRACTURE ( 17 FDA reports)
ASCITES ( 17 FDA reports)
BREATH ODOUR ( 17 FDA reports)
CACHEXIA ( 17 FDA reports)
CHOLELITHIASIS ( 17 FDA reports)
COMPRESSION FRACTURE ( 17 FDA reports)
DISABILITY ( 17 FDA reports)
DRY EYE ( 17 FDA reports)
DRY MOUTH ( 17 FDA reports)
DUODENITIS ( 17 FDA reports)
FACIAL PAIN ( 17 FDA reports)
HEART RATE IRREGULAR ( 17 FDA reports)
HEPATITIS ( 17 FDA reports)
HYPERTENSION ( 17 FDA reports)
HYPERTHYROIDISM ( 17 FDA reports)
HYPOVOLAEMIA ( 17 FDA reports)
INSOMNIA ( 17 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 17 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 17 FDA reports)
JAUNDICE ( 17 FDA reports)
JOINT SWELLING ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
MALNUTRITION ( 17 FDA reports)
MUCOSAL INFLAMMATION ( 17 FDA reports)
MUSCLE STRAIN ( 17 FDA reports)
OSTEOMYELITIS CHRONIC ( 17 FDA reports)
OSTEONECROSIS OF JAW ( 17 FDA reports)
OSTEOPENIA ( 17 FDA reports)
OSTEOPOROSIS ( 17 FDA reports)
PERIODONTAL DISEASE ( 17 FDA reports)
RENAL FAILURE CHRONIC ( 17 FDA reports)
RIB FRACTURE ( 17 FDA reports)
SINUS CONGESTION ( 17 FDA reports)
SINUS TACHYCARDIA ( 17 FDA reports)
STOMATITIS ( 17 FDA reports)
SWELLING FACE ( 17 FDA reports)
TINNITUS ( 17 FDA reports)
VITAMIN A DEFICIENCY ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
DEAFNESS ( 16 FDA reports)
EAR PAIN ( 16 FDA reports)
EPISTAXIS ( 16 FDA reports)
FEELING ABNORMAL ( 16 FDA reports)
PARAESTHESIA ( 16 FDA reports)
TOOTH INFECTION ( 16 FDA reports)
ALOPECIA ( 15 FDA reports)
ANAEMIA ( 15 FDA reports)
ANOREXIA NERVOSA ( 15 FDA reports)
BONE DENSITY DECREASED ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
BONE PAIN ( 15 FDA reports)
CRANIAL NERVE DISORDER ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
ENDOCRINE DISORDER ( 15 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
FAILURE TO THRIVE ( 15 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 15 FDA reports)
HYPERALDOSTERONISM ( 15 FDA reports)
HYPOMETABOLISM ( 15 FDA reports)
IMMUNODEFICIENCY ( 15 FDA reports)
NASAL ULCER ( 15 FDA reports)
PINEAL GLAND CYST ( 15 FDA reports)
RAYNAUD'S PHENOMENON ( 15 FDA reports)
RHINITIS ( 15 FDA reports)
SCOLIOSIS ( 15 FDA reports)
SIALOADENITIS ( 15 FDA reports)
TIBIA FRACTURE ( 15 FDA reports)
VITAMIN C DEFICIENCY ( 15 FDA reports)
VITAMIN D DEFICIENCY ( 15 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
CHOLECYSTITIS CHRONIC ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
VERTEBRAL WEDGING ( 14 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
KIDNEY MALROTATION ( 13 FDA reports)
OSTEOCHONDROSIS ( 13 FDA reports)
OSTEOMALACIA ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
VOMITING ( 13 FDA reports)
NECK PAIN ( 12 FDA reports)
DIARRHOEA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
GALLBLADDER DISORDER ( 11 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
PYREXIA ( 9 FDA reports)
BILIARY DYSKINESIA ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
AMENORRHOEA ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
COLITIS ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
GALLBLADDER INJURY ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
RASH ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
VACCINATION SITE INFLAMMATION ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHOLESTEROSIS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FEAR ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OVARIAN DISORDER ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COUGH ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
SMALL INTESTINAL STENOSIS ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)

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