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

SEPSIS ( 17 FDA reports)
PYREXIA ( 14 FDA reports)
COLITIS ( 13 FDA reports)
RASH ( 12 FDA reports)
NAUSEA ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
CYSTITIS HAEMORRHAGIC ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
BLISTER ( 6 FDA reports)
BURNING SENSATION ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
CHILLS ( 5 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
PAIN ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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