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

PAIN ( 26 FDA reports)
DYSPNOEA ( 25 FDA reports)
ARTHRALGIA ( 20 FDA reports)
HEADACHE ( 20 FDA reports)
NAUSEA ( 20 FDA reports)
CONSTIPATION ( 18 FDA reports)
VISION BLURRED ( 18 FDA reports)
ANAEMIA ( 17 FDA reports)
DEPRESSION ( 17 FDA reports)
DIARRHOEA ( 16 FDA reports)
FALL ( 16 FDA reports)
FATIGUE ( 16 FDA reports)
RASH ( 16 FDA reports)
BACK PAIN ( 15 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
DENTAL CARIES ( 15 FDA reports)
PULMONARY EMBOLISM ( 15 FDA reports)
HYPERTENSION ( 14 FDA reports)
PARAESTHESIA ( 14 FDA reports)
URINARY TRACT INFECTION ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
DIPLOPIA ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
HIATUS HERNIA ( 13 FDA reports)
HYPOGLYCAEMIA ( 13 FDA reports)
LUNG NEOPLASM ( 13 FDA reports)
OSTEONECROSIS OF JAW ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
SINUSITIS ( 13 FDA reports)
SKIN DISORDER ( 13 FDA reports)
TOOTH DISORDER ( 13 FDA reports)
ULCER ( 13 FDA reports)
VISUAL IMPAIRMENT ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
DIZZINESS ( 12 FDA reports)
HOT FLUSH ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
NASAL CONGESTION ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
WITHDRAWAL SYNDROME ( 12 FDA reports)
COUGH ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
GINGIVAL DISORDER ( 11 FDA reports)
HEAD INJURY ( 11 FDA reports)
JOINT SWELLING ( 11 FDA reports)
LACRIMATION INCREASED ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
ABSCESS NECK ( 10 FDA reports)
ACCOMMODATION DISORDER ( 10 FDA reports)
ADENOMYOSIS ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 10 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 10 FDA reports)
APHASIA ( 10 FDA reports)
ARTHROPATHY ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
ATAXIA ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
CHEMICAL POISONING ( 10 FDA reports)
COCCYDYNIA ( 10 FDA reports)
COLITIS ( 10 FDA reports)
EXCORIATION ( 10 FDA reports)
EYE PAIN ( 10 FDA reports)
FACIAL PAIN ( 10 FDA reports)
GINGIVAL PAIN ( 10 FDA reports)
HEPATIC STEATOSIS ( 10 FDA reports)
HEPATOMEGALY ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
HYPOXIA ( 10 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 10 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 10 FDA reports)
IRON DEFICIENCY ANAEMIA ( 10 FDA reports)
JAW DISORDER ( 10 FDA reports)
LABYRINTHITIS ( 10 FDA reports)
LACERATION ( 10 FDA reports)
LYMPHOEDEMA ( 10 FDA reports)
MICROCYTIC ANAEMIA ( 10 FDA reports)
MIGRAINE ( 10 FDA reports)
MOUTH ULCERATION ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
NEPHROLITHIASIS ( 10 FDA reports)
NEURODERMATITIS ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
OESOPHAGITIS ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
RETINOPATHY ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
TONGUE INJURY ( 10 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 10 FDA reports)
URETERAL DISORDER ( 10 FDA reports)
UTERINE HAEMORRHAGE ( 10 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
VITREOUS FLOATERS ( 10 FDA reports)
WOUND ( 10 FDA reports)
WOUND HAEMORRHAGE ( 10 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
VOMITING ( 9 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
WEST NILE VIRAL INFECTION ( 8 FDA reports)
ARTHRITIS ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
DRY MOUTH ( 6 FDA reports)
INJURY ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
AGGRESSION ( 5 FDA reports)
AGITATION ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MYELOPATHY ( 5 FDA reports)
OBESITY ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SUICIDAL BEHAVIOUR ( 5 FDA reports)
TOOTH ABSCESS ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BONE LOSS ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABSCESS JAW ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAL SKIN TAGS ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DUODENAL STENOSIS ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INFECTION ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LOOSE TOOTH ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RECTAL ULCER ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
SCOLIOSIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TENSION HEADACHE ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC FOOT ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VASCULAR CALCIFICATION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MASS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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