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SYNCOPE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
LIGAMENT INJURY ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
FALL ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DEPRESSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COMA ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PAIN ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RALES ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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