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

FALL ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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