Humate and hypersensitivity Patient Reports February 12, 2012

Humate Side Effects Report #5650210-0
Humate side effect was reported by a Consumer or non-health professional from CANADA on Feb 19, 2008. Female patient, 58 years of age, weighting 187.0 lb, was diagnosed with von willebrand's disease and was treated with Humate. After drug was administered, patient experienced the following side effects: blood sodium decreased, dyspnoea, fluid retention, hypersensitivity, insomnia, localised oedema, oedema peripheral, pruritus, rales. Humate dosage: unknown. During the same period patient was treated with DICLOFENAC, CIPRO, FLUTICASONE, CLONAZEPAM, DOMPERIDONE, ESOMEPRAZOLE MAGNESIUM, CITALOPRAM, BUPROPION. Patient recovered.

Humate Side Effects Report #5443004-2
Humate side effect was reported by a Consumer or non-health professional from CANADA on Aug 10, 2007. Female patient, 58 years of age, weighting 187.0 lb, was diagnosed with surgery , von willebrand's disease and was treated with Humate. After drug was administered, patient experienced the following side effects: fluid retention, hypersensitivity, insomnia, pulmonary oedema, venous pressure jugular increased, weight increased. Humate dosage: unknown. During the same period patient was treated with DICLOFENAC, CIPRO, FLUTICASONE PROPIONATE, CLONAZEPAM, DOMPERIDONE, ESOMEPRAZOLE MAGNESIUM, CITALOPRAM HYDROBROMIDE. Patient recovered.