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

FALL ( 4 FDA reports)
HIP FRACTURE ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
FEAR ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PAIN ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)

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