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MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
FALL ( 4 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
UVEITIS ( 1 FDA reports)

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