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

PAIN ( 32 FDA reports)
PAIN IN EXTREMITY ( 22 FDA reports)
HYPERTENSION ( 18 FDA reports)
DIZZINESS ( 17 FDA reports)
MALAISE ( 17 FDA reports)
FALL ( 16 FDA reports)
OEDEMA PERIPHERAL ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
FATIGUE ( 15 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
ERYTHEMA ( 13 FDA reports)
DRY SKIN ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
VOMITING ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
ALOPECIA ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
BONE PAIN ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
INFLUENZA ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
ABASIA ( 7 FDA reports)
ACROMEGALY ( 7 FDA reports)
BLINDNESS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
COUGH ( 7 FDA reports)
HAIR DISORDER ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
SPINAL DISORDER ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 5 FDA reports)
MULTIPLE SCLEROSIS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
COMA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
SURGERY ( 4 FDA reports)
THIRST ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONNECTIVE TISSUE DISORDER ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
MEDICAL DEVICE CHANGE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RHEUMATIC FEVER ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
VARICOSE VEIN ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACHOLIA ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN TUMOUR OPERATION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
POLYP ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACNE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SYMPHYSIOLYSIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use