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PATHOLOGICAL FRACTURE ( 13 FDA reports)
RASH PUSTULAR ( 7 FDA reports)
LEUKOCYTOSIS ( 7 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
TIBIA FRACTURE ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
FRACTURE DELAYED UNION ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)

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