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INFLUENZA LIKE ILLNESS ( 22 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 19 FDA reports)
FALL ( 15 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
PAIN ( 9 FDA reports)
HYPERTENSION ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
ARTHRITIS ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
CORONARY ARTERY OCCLUSION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COMA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
RASH ( 3 FDA reports)
SPLENIC RUPTURE ( 3 FDA reports)
STRESS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MENINGITIS HERPES ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCINTILLATING SCOTOMA ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE II ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLPOCELE ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMOID CYST OF OVARY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS INCONTINENCE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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