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

FATIGUE ( 7 FDA reports)
SYNCOPE ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FALL ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BLOOD CALCIUM 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 SODIUM DECREASED ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 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)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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