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

INSOMNIA ( 14 FDA reports)
HALLUCINATION ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
SOMNOLENCE ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
FALL ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
LIBIDO DECREASED ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
FEAR ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSCILLOPSIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
FOOD CRAVING ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUROMUSCULAR BLOCKADE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
STRESS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VEIN DISORDER ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASTEATOSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use