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

NAUSEA ( 4 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMENTIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
STRESS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)

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