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

DIZZINESS ( 5 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
HEAD INJURY ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
FALL ( 2 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)

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