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FATIGUE ( 5 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FALL ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCLEROMALACIA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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