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

ANXIETY ( 18 FDA reports)
FALL ( 16 FDA reports)
PNEUMONIA ( 16 FDA reports)
FATIGUE ( 14 FDA reports)
NAUSEA ( 12 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
DEATH ( 11 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BRAIN CONTUSION ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SNORING ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
APATHY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CLUSTER HEADACHE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
MOEBIUS II SYNDROME ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
POISONING ( 3 FDA reports)
POLAND'S SYNDROME ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
TALIPES ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEXTROCARDIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTONIA NEONATAL ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PRADER-WILLI SYNDROME ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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