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

MULTI-ORGAN FAILURE ( 17 FDA reports)
PANCREATITIS ACUTE ( 17 FDA reports)
HYPOGLYCAEMIA ( 15 FDA reports)
ANGIOEDEMA ( 11 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
DRY SKIN ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
WITHDRAWAL SYNDROME ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
FALL ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
AURA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
THROMBOLYSIS ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RALES ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)

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