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

ANXIETY ( 17 FDA reports)
DEPRESSION ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
HAEMORRHOIDS ( 13 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
PAIN ( 11 FDA reports)
RHEUMATOID ARTHRITIS ( 11 FDA reports)
HYPERLIPIDAEMIA ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
COUGH ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
BACK PAIN ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
JAW FRACTURE ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ANGER ( 6 FDA reports)
ANTICOAGULANT THERAPY ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BENIGN NEOPLASM OF SKIN ( 6 FDA reports)
CALCIUM DEFICIENCY ( 6 FDA reports)
COLITIS ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CROHN'S DISEASE ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
EMBOLISM ( 6 FDA reports)
ENTERITIS ( 6 FDA reports)
FAECAL INCONTINENCE ( 6 FDA reports)
FALL ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 6 FDA reports)
INTESTINAL STENOSIS ( 6 FDA reports)
LARGE INTESTINAL ULCER ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
LOWER LIMB FRACTURE ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MIXED INCONTINENCE ( 6 FDA reports)
OSTEOPENIA ( 6 FDA reports)
PARATHYROID DISORDER ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SEBACEOUS GLAND DISORDER ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SKIN DISORDER ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
URETHRAL CARUNCLE ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
DEATH ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
DYSTHYMIC DISORDER ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
INJURY ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
SWELLING ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FEAR ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
STRESS ( 3 FDA reports)
TOOTH FRACTURE ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEURILEMMOMA BENIGN ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
ORAL FIBROMA ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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