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

ARTHRALGIA ( 44 FDA reports)
HEADACHE ( 39 FDA reports)
FALL ( 38 FDA reports)
MULTIPLE SCLEROSIS ( 32 FDA reports)
INJECTION SITE PAIN ( 31 FDA reports)
TREMOR ( 31 FDA reports)
DIZZINESS ( 30 FDA reports)
MUSCULAR WEAKNESS ( 30 FDA reports)
PYREXIA ( 30 FDA reports)
URINARY INCONTINENCE ( 30 FDA reports)
GAIT DISTURBANCE ( 29 FDA reports)
MALAISE ( 29 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 27 FDA reports)
INFLUENZA ( 26 FDA reports)
JOINT SWELLING ( 25 FDA reports)
DIPLOPIA ( 24 FDA reports)
PAIN ( 24 FDA reports)
BALANCE DISORDER ( 23 FDA reports)
CONSTIPATION ( 23 FDA reports)
DYSPHONIA ( 23 FDA reports)
EYE MOVEMENT DISORDER ( 23 FDA reports)
MENSTRUAL DISORDER ( 23 FDA reports)
HELMINTHIC INFECTION ( 20 FDA reports)
INJURY ( 20 FDA reports)
NAUSEA ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
DEPRESSION ( 15 FDA reports)
FATIGUE ( 12 FDA reports)
PRODUCTIVE COUGH ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
BURNING SENSATION ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
SPEECH DISORDER ( 9 FDA reports)
MOTOR DYSFUNCTION ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
UNEVALUABLE EVENT ( 8 FDA reports)
ALOPECIA ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
INCREASED BRONCHIAL SECRETION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
ARTHRITIS ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CHOKING ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
VOMITING ( 6 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
MUSCLE CONTRACTURE ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CRYING ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
SWELLING ( 4 FDA reports)
UTERINE NEOPLASM ( 4 FDA reports)
ACNE ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
JOINT SPRAIN ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
POLYMYOSITIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY TRACT INJURY ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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