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

ANXIETY ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
DIZZINESS ( 7 FDA reports)
VISION BLURRED ( 6 FDA reports)
SEDATION ( 6 FDA reports)
PAIN ( 6 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SALIVARY GLAND CALCULUS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
ASCITES ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
LENS IMPLANT ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
DEATH ( 2 FDA reports)
TREMOR ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
STRESS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NAUSEA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use