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

DYSPNOEA ( 26 FDA reports)
NAUSEA ( 25 FDA reports)
PAIN ( 22 FDA reports)
VOMITING ( 20 FDA reports)
ASTHMA ( 19 FDA reports)
PULMONARY EMBOLISM ( 19 FDA reports)
ABDOMINAL PAIN UPPER ( 17 FDA reports)
DEEP VEIN THROMBOSIS ( 15 FDA reports)
DIZZINESS ( 15 FDA reports)
HEADACHE ( 14 FDA reports)
CHOLECYSTITIS CHRONIC ( 13 FDA reports)
GALLBLADDER DISORDER ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
ANXIETY ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
BACK PAIN ( 11 FDA reports)
MALAISE ( 11 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
PARAESTHESIA ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
DEATH ( 7 FDA reports)
FALL ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ANGER ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
FEELING JITTERY ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
INJURY ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OPHTHALMOPLEGIA ( 5 FDA reports)
PULMONARY INFARCTION ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
TOXIC NEUROPATHY ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ADRENALITIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
STRESS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPNAGOGIC HALLUCINATION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TIC ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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