Fondaparinux and haemoglobin decreased Patient Reports February 12, 2012
Fondaparinux Side Effects Report #4843834-1
Fondaparinux side effect was reported by a Consumer or non-health professional from NETHERLANDS on June 27, 2005. Female patient, 79 years of age, was diagnosed with thrombosis prophylaxis and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: anaemia, atrial fibrillation
, blood pressure systolic increased, haemoglobin decreased, operative haemorrhage, platelet count decreased, shock haemorrhagic. Fondaparinux dosage: unknown. Patient recovered.Fondaparinux Side Effects Report #5104280-9
Fondaparinux side effect was reported by a Pharmacist from UNITED STATES on Sept 12, 2006. Male patient was diagnosed with thrombosis prophylaxis and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased. Fondaparinux dosage: 2.5 MG DAILY SQ. During the same period patient was treated with ACETAMINOPHEN AND HYDROCODONE BITARTRATE, ALBUTEROL, DIPHENHYDRAMINE, DOCUSATE, DOXEPIN, FLUNISOLIDE ORAL INHALANT, FORADIL, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Fondaparinux Side Effects Report #5107566-7
Fondaparinux side effect was reported by a Pharmacist from UNITED STATES on Sept 13, 2006. Male patient was diagnosed with thrombosis prophylaxis and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased. Fondaparinux dosage: 2.5 MG DAILY SQ. During the same period patient was treated with APAP, ALBUTEROL, CEFAZOLIN, DIPHENHYDRAMINE, FELODIPINE, HYDROCHLOROTHIAZIDE, OXYCODONE AND ACETAMINOPHEN, POTASSIUM CHLORIDE. Patient was hospitalized. Patient recovered.
Fondaparinux Side Effects Report #5107575-8
Fondaparinux side effect was reported by a Pharmacist from UNITED STATES on Sept 13, 2006. Male patient was diagnosed with thrombosis prophylaxis and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased. Fondaparinux dosage: 2.5 MG DAILY SQ. During the same period patient was treated with ALBUTEROL, DIPHENHYDRAMINE, DOCUSATE, FLUNISOLIDE ORAL, GABAPENTIN, IPRATROPIUM BROMIDE, MONTELUKAST, OXYCODONE AND ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Fondaparinux Side Effects Report #4763699-6
Fondaparinux side effect was reported by a Physician from NETHERLANDS on Dec 13, 2004. Female patient, 84 years of age, was diagnosed with orthopedic procedure and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased, platelet count increased, post procedural haemorrhage, staphylococcal infection
, white blood cell count increased, wound infection. Fondaparinux dosage: 2.5MG PER DAY. During the same period patient was treated with ACENOCOUMAROL. Patient was hospitalized. Patient recovered.Fondaparinux Side Effects Report #4888300-2
Fondaparinux side effect was reported by a Physician from CANADA on Jan 19, 2006. Male patient, 65 years of age, was diagnosed with myocardial infarction and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: artery dissection, haemoglobin decreased, post procedural haemorrhage, procedural complication. Fondaparinux dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN, HEPARIN. Patient was hospitalized. Patient recovered.
Fondaparinux Side Effects Report #4886160-7
Fondaparinux side effect was reported by a Physician from CANADA on Jan 18, 2006. Male patient, 78 years of age, weighting 196.2 lb, was diagnosed with acute myocardial infarction and was treated with Fondaparinux. After drug was administered, patient experienced the following side effects: anaemia, anaemia macrocytic, haemoglobin decreased, myelodysplastic syndrome, renal impairment. Fondaparinux dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN, UNFRACTIONATED HEPARIN. Patient recovered.
Fondaparinux and haemoglobin decreased 