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INFLUENZA LIKE ILLNESS ( 25 FDA reports)
MULTIPLE SCLEROSIS ( 24 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
CORONARY ARTERY OCCLUSION ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
CHEST PAIN ( 9 FDA reports)
CHILLS ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
THROAT TIGHTNESS ( 9 FDA reports)
FEELING HOT ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
EMOTIONAL DISORDER ( 7 FDA reports)
FALL ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
INFUSION RELATED REACTION ( 7 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 7 FDA reports)
LATEX ALLERGY ( 7 FDA reports)
RASH ( 7 FDA reports)
SWELLING ( 7 FDA reports)
VOMITING ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
PAIN ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COMA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SURGERY ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RENAL ADENOMA ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THORACIC OUTLET SYNDROME ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OSTEOARTHRITIS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)

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