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

NAUSEA ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 7 FDA reports)
MYALGIA ( 6 FDA reports)
DEFORMITY ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
LICHENIFICATION ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
PEAU D'ORANGE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SCAR ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN HYPERTROPHY ( 5 FDA reports)
SKIN HYPOPIGMENTATION ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
SKIN TIGHTNESS ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
VOMITING ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FALL ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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