Menu

• Ask a Health Expert about HYPOCOAGULABLE STATE
• Post Your Side Effect related to HYPOCOAGULABLE STATE
• HYPOCOAGULABLE STATE and FDA Warnings
• HYPOCOAGULABLE STATE in Patients Wiki
• Report HYPOCOAGULABLE STATE in Drug Side Effect Survey

HYPOCOAGULABLE STATE side effect

What is HYPOCOAGULABLE STATE ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Letairis Side Effects Report #5662207-5
Pharmacist from UNITED STATES reported LETAIRIS problem on Mar 06, 2008. Female patient, weighting 192.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, hypocoagulable state, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, LASIX, SPIRONOLACTONE, BENICAR, COUMADIN, ALLOPURINOL, ACTONEL. Patient was hospitalized. Patient recovered.

Letairis Side Effects Report #5671186-6
LETAIRIS problem was reported by a Pharmacist from UNITED STATES on Mar 12, 2008. Female patient, weighting 192.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, hypocoagulable state, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, LASIX, SPIRONOLACTONE, BENICAR, COUMADIN, ALLOPURINOL, ACTONEL. Patient was hospitalized. Patient recovered.

Letairis Side Effects Report #5679656-1
Physician from UNITED STATES reported LETAIRIS problem on Mar 20, 2008. Female patient, weighting 192.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, hypocoagulable state, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, LASIX, SPIRONOLACTONE, BENICAR, COUMADIN, ALLOPURINOL, ACTONEL. Patient was hospitalized. Patient recovered.

Letairis Side Effects Report #5685275-3
LETAIRIS problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 26, 2008. Female patient, weighting 192.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, hypocoagulable state, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, LASIX, SPIRONOLACTONE, BENICAR, COUMADIN, ALLOPURINOL, ACTONEL. Patient was hospitalized. Patient died on 03/14/2008.


Arixtra Side Effects Report #5504183-1
Physician from JAPAN reported ARIXTRA problem on Oct 26, 2007. Male patient, 72 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: atelectasis, disseminated intravascular coagulation, hypocoagulable state, oxygen saturation decreased, pneumonia, puncture site haemorrhage, respiratory arrest, respiratory disorder, respiratory tract congestion, . ARIXTRA dosage: 2.5MG PER DAY. Patient died on 08/22/2007.

Revlimid Side Effects Report #5481052-7
REVLIMID problem was reported by a Physician from UNITED STATES on Sept 28, 2007. Female patient, 87 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: arterial thrombosis, arteriosclerosis, hypocoagulable state, pedal pulse decreased, peripheral ischaemia, poor peripheral circulation, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. During the same period patient was treated with ACTIVASE, CLOPIDOGREL, ASPIRIN. Patient was hospitalized. Patient died.

Arixtra Side Effects Report #5482390-4
Physician from JAPAN reported ARIXTRA problem on Oct 09, 2007. Male patient, 72 years of age, was diagnosed with spinal cord injury cervical and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: atelectasis, disseminated intravascular coagulation, hypocoagulable state, oxygen saturation decreased, pneumonia, puncture site haemorrhage, respiratory arrest, respiratory disorder, respiratory tract congestion, . ARIXTRA dosage: 2.5MG PER DAY. Patient died on 08/22/2007.

Quinidine Side Effects Report #5413119-3
QUINIDINE SULPHATE problem was reported by a Health Professional from FRANCE on July 31, 2007. Female patient, 68 years of age, was diagnosed with arrhythmia and was treated with QUINIDINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: anti-prothrombin antibody positive, antiphospholipid antibodies, hypocoagulable state, hypoprothrombinaemia, . QUINIDINE SULPHATE dosage: unknown. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5301798-0
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on Apr 16, 2007. Female patient, weighting 162.3 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis, fatigue, hypocoagulable state, malignant neoplasm progression, myalgia, no therapeutic response, . CARBOPLATIN dosage: 440 MG. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.


Remicade Side Effects Report #5257245-0
REMICADE problem was reported by a Physician from FRANCE on Mar 01, 2007. Male patient, 63 years of age, weighting 154.3 lb, was diagnosed with crohn's disease, atrial fibrillation and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: haematuria, hypocoagulable state, international normalised ratio increased, subcutaneous haematoma, . REMICADE dosage: unknown. During the same period patient was treated with PREVISCAN, ATACAND. Patient recovered.