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Dennis Quaid and wife sue drug maker
Rodert Jablon
LOS ANGELES—Dennis Quaid and his wife sued the makers of heparin Tuesday
after their newborn twins were inadvertently given massive doses of the
blood thinner at a hospital.
The product liability lawsuit, filed in Chicago, seeks more than $50,000
in damages. It claims that Baxter Healthcare Corp., based in Deerfield,
Ill., was negligent in packaging different doses of the product in
similar vials with blue backgrounds. The lawsuit also says the company
should have recalled the large-dosage vials after overdoses killed three
children at an Indianapolis hospital last year.
The lawsuit was first reported by CelebTV.com, which obtained the court
documents. The company had not been served with the lawsuit and could
not comment specifically on it, spokeswoman Deborah Spak said. However,
“this is not a product issue. The issue here is about improper use of a
product,” she said. “While we strive to clearly differentiate our
products and dosages, no amount of differentiation will replace the
value of clinicians carefully reviewing and reading a drug name and dose
before dispensing and administering it,” she added.
This fall, the company changed its heparin packaging by adding a red
caution label that must be torn off before the vial can be opened. The
Quaids’ children, Thomas Boone and Zoe Grace, and a third patient were
at Cedars-Sinai Medical Center on Nov. 18 when they were mistakenly
given vials of heparin that were 1,000 times stronger than the usual
dosage.
Cedars-Sinai said Tuesday the mistake occurred when two pharmacy
technicians failed to verify the vials’ concentration before placing
them in the pediatrics unit where the lower-concentration heparin is
kept. The nurses who administered the drug also failed to check the
dosage, the hospital said in a news release. The issued an apology to
the patients’ families and said it has made a series of changes to
prevent a recurrence, including providing more training to staff and
requiring four pharmacy workers to verify a “high-alert” medication
before putting it in a patient care unit.
The twins were home Tuesday and “appear to be doing well,” said Susan E.
Loggans, the Chicago attorney who filed the lawsuit. “The Quaids are a
religious family, and they really believe the prayers of the public
saved their kids.” “Apparently, they’re going to be fine now,” she said
but declined to otherwise comment on the children’s medical conditions.
“The point of this case is to save other children from this fate.
They’re not looking for money,” Loggans said of the lawsuit. The Quaids
didn’t sue Cedars-Sinai, which acknowledged after the news broke that a
“preventable error” had resulted in three patients receiving vials
containing 10,000 units per milliliter of heparin instead of vials with
a concentration of 10 units per milliliter.
The patients were receiving intravenous medications and the heparin was
used to flush the catheters to prevent clotting. Two of the patients
needed a drug that reverses the effects of heparin, the hospital said at
the time.
The hospital issued an apology to the patients’ families, and said it
would take “all steps” to prevent a recurrence. The heparin was
“unreasonably dangerous” as it was packaged and sold because both the
small and large dosage vials had labels with blue backgrounds when the
vials “should have been completely distinguishable (by) size and shape,”
the lawsuit argued.
A similar dosage error killed three premature infants at an Indianapolis
hospital last year. Three others survived overdoses. |