Heparin Recall Linked To Deaths

Heparin, a blood thinner manufactured by Baxter, has apparently been linked to up to 62 deaths as of April of 2008.

In January of 2008, Baxter announced a voluntary recall of all multi dose vials of Heparin from a certain nine lots.

In February, Baxter announced a recall of all Heparin in hospitals and surgery centers nationwide.

As of April, 2008, more than 62 deaths were allegedly linked to Heparin as we as 350 allergic reactions to the blood thinner. Allergic reactions appear linked to the amount of dosage with higher amounts resulting in more serious side effects.

Adverse side effects include: stomach pain; shortness of breath; nausea; throat swelling; low blood pressure; chest pain; accelerated heart rate; dizziness; headaches; restlessness; dizziness; vomiting; diarrhea; fainting; unresponsiveness; tachycardia; drug ineffectiveness; burning sensations; redness or paleness of skin; abnormal sensation of the skin, mouth, or lips; flushing; thirst and difficulty opening the mouth, increased sweating; decreased skin sensitivity; watery eyes; and low blood pressure.

The apparent cause of the Heparin reaction is linked to the manufacture of the blood thinner overseas.

Heparin has been in use in the United States for over 70 years and before the recall, more than 100,000 doses were delivered daily.

Baxter can be found on the web at www.baxter.com.