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

CONVULSION ( 12 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 10 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 10 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
HEADACHE ( 4 FDA reports)
INFECTION ( 4 FDA reports)
PAIN ( 4 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PARALYSIS ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
FALL ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use