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

HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
KAPOSI'S SARCOMA ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
HYPERLACTACIDAEMIA ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RASH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)

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