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

PERITONITIS ( 4 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
CLONUS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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