Humate and dyspnoea 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 #5794367-X
Humate side effect was reported by a Physician from UNITED STATES on June 06, 2008. Female patient, 37 years of age, weighting 288.0 lb, was diagnosed with von willebrand's disease and was treated with Humate. After drug was administered, patient experienced the following side effects: catheter sepsis, cyanosis, dyspnoea, hyperhidrosis, muscle rigidity, muscle spasms, pyrexia, tremor, urinary tract infection . Humate dosage: unknown. Patient died on 06/06/2008.

Humate Side Effects Report #5820050-8
Humate side effect was reported by a Physician from UNITED STATES on July 04, 2008. Female patient, 37 years of age, weighting 288.0 lb, was diagnosed with von willebrand's disease and was treated with Humate. After drug was administered, patient experienced the following side effects: body temperature increased, catheter related infection, culture positive, cyanosis, dyspnoea, hyperhidrosis, infusion related reaction, muscle rigidity, muscle spasms. Humate dosage: unknown. Patient died on 06/06/2008.