Thomas v. Smithkline Beecham Corp.

27 Pa. D. & C.5th 279
CourtPennsylvania Court of Common Pleas, Philadelphia County
DecidedNovember 9, 2012
DocketNo. 3527, 2007 Superior Court No. 2461 EDA 2012
StatusPublished

This text of 27 Pa. D. & C.5th 279 (Thomas v. Smithkline Beecham Corp.) is published on Counsel Stack Legal Research, covering Pennsylvania Court of Common Pleas, Philadelphia County primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Thomas v. Smithkline Beecham Corp., 27 Pa. D. & C.5th 279 (Pa. Super. Ct. 2012).

Opinion

MOSS, J.,

Plaintiff, JoAnne Thomas, individually and as parent and natural guardian of Ryan Swindle, appeals this court’s order dated July 17, 2012, and docketed July 19, 2012, granting defendant, SmithKline Beecham Corporation (“GSK”), summary judgment based on non-viability of the fetus and applicable statute of limitations. For the following reasons, our order should be affirmed.

I. BACKGROUND

The facts in a light most favorable to plaintiff follow. Plaintiff, JoAnne Thomas, instituted this action by writ of summons on September 25, 2007. On November 27, 2007, plaintiff filed a short-form complaint. Plaintiff was allegedly taking a 40mg dose of Paxil (Paroxetine) throughout her pregnancy with Ryan Swindle in 2001. See defendant’s motion, 3/22/12, p.3. At the time, Paxil was classified as a category C drug by the FDA drug use in pregnancy ratings. See “Understanding Antidepressant Medications, ” U.S. Food and Drug Administration: Consumer Health Info, January 9, 2009, available at http://www.fda.gov/ForConsumers/ConsumerUpdates/ ucm095980.htm (last visited Oct. 12,2012). In December 2005, the FDA reclassified Paxil from a pregnancy risk category of C to D. Id. See also, U.S. food and drug administration, FDA Advising of Risk of Birth Defects With Paxil, Agency Requiring Updated Product Labeling, December 8, 2005, available at http://www.fda.gov/ [282]*282NewsEvents/Newsroom/PressAnnouncements/2005/ ucml08527.htm (last visited Oct. 12, 2012). “With a Category C drag, fetal risk cannot be ruled out. With a Category D drag, positive evidence of fetal risks exists. FDA chooses a medicine’s letter category based on what is known about the medicine when used in pregnant women and animals.” Id.

In plaintiff’s last echocardiogram performed on April 23, 2001, the pediatric cardiologist estimated fetal gestational age to be 22 1/2 weeks, and notified her of baby’s congenital heart defects. See plaintiff’s response, exhibit 1, fetal echocardiogram report (4/23/01). What caused said fetal abnormalities was unknown and the doctor suggested a following up in 5-6 weeks. Id. On April 26, 2001, 3 days later, plaintiff voluntarily chose a therapeutic abortion. See defendant’s motion, exhibit 2, fetal death certificate. The fetal death certificate estimated gestational age to be 21 1/2 weeks. Id.

On March 8,2007, nearly six years later, while plaintiff was studying for her nursing boards, she contacted a consumer line on GSK’s website and spoke with a customer service representative who incorrectly told her Paxil was a “category C” drag. See defendant’s reply, exhibit 2, Amended pregnancy fact sheet (12/9/10). With further investigation, plaintiff discovered Paxil had moved from a category C to D drag. See “Understanding Antidepressant Medications, ” U.S. Food and Drug Administration: Consumer Health Info. (2009). The representative later confirmed Paxil had been relabeled a category D drag. See plaintiff’s response, exhibit 2, affidavit of JoAnne Thomas (4/20/12). Plaintiff then filed her short form complaint November 27,2007, alleging her [283]*283Paxil ingestion during pregnancy caused her son, Ryan Swindle’s wrongful death. Defendant’s motion, exhibit 1, short form complaint, ¶6 (11/27/07).

On March 22, 2012, GSK moved for summary judgment. GSK argued plaintiff’s claims should be dismissed for two fundamental reasons. First, plaintiff cannot bring a wrongful death or survival action because her fetus was not viable at her therapeutic abortion.1 See defendant’s motion, p.2. GSK argues as a matter of law there must be either (1) a child bom alive; or (2) a viable fetus, capable of an independent existence at death. See Coveleski v. Bubnis, 535 Pa. 166, 172, 634 A.2d 608, 610 (1993). Under Pennsylvania law, viability occurs no earlier than 23 weeks gestational age. See McCaskill v. Phila. Housing Auth., 615 A.2d 382, 384 (Pa. Super. Ct. 1992) (following the U.S. Supreme Court’s holding in Planned Parenthood v. Casey, 505 U.S. 833, 860 (1992), that viability occurs at 23 to 24 weeks). Relying on plaintiff’s fetal death certificate, GSK argued she cannot sustain a wrongful death or survival action because she at 21 1/2 weeks, before viability occurred. See defendant’s motion, exhibit 2, fetal death certificate.

Next, GSK argued even if the fetus was viable when aborted, any claim would be barred under Pennsylvania’s two year statute of limitations because plaintiff filed her action November 27, 2007, more than 6 years its death. GSK contends the two-year period commenced on the day [284]*284Ryan Swindle died, regardless of when survivors knew, or should have known, cause of death. See defendant’s motion, p.4.

Plaintiff answered April 23, 2012, arguing at time of death, fetal gestational age was approximately 23 weeks, which is the viability threshold Pennsylvania courts recognize. See plaintiff’s response, p.4. Three days before Ryan Swindle died, a pediatric cardiologist estimated fetal gestational age at 22 1/2 weeks. See plaintiff’s response, Exhibit 1, fetal echocardiogram report (4/23/01). Plaintiff argued if viability threshold is 23 weeks, the echocardiogram report creates a genuine issue of fact as to whether Ryan Swindle was viable when aborted. Plaintiff also argues said statute should be equitably tolled under the doctrine of fraudulent concealment. Plaintiff argued GSK’s safety misrepresentations hindered her ability to discover what caused the birth defects prior and subsequent to said abortion. See plaintiff’s response, p.5. Plaintiff asserts whether GSK fraudulently concealed pregnancy risks associated with Paxil is a jury question. Id.

Defendant replied on April 30, 2012, reiterating plaintiff cannot bring a wrongful death or survival action because the fetus was not viable as a matter of law. See defendant’s reply, p. 2. Even if plaintiff was 22 1/2 weeks pregnant three days before the abortion, her claim she was “approximately” 23 weeks is simply not enough to establish viability under Pennsylvania’s bright-line rule. See defendant’s reply, executive summary. Plaintiff elected to terminate her pregnancy just prior to the critical point when viability occurs. Id.

GSK further argued plaintiff fails to establish fraudulent [285]*285concealment and largely repeats her overarching “failure to warn claims” rather than establishing evidence that GSK committed “an affirmative, independent act of concealment directed towards plaintiff upon which she justifiably relied.” See defendant’s reply, p.3. Plaintiff cannot establish any specific “act” of GSK caused her to relax vigilance or deviate from inquiring. Id. The only potentially responsive argument plaintiff makes is she allegedly called the GSK consumer response center in March 2007. However, the statute had already expired by the time she allegedly called. See defendant’s reply, p.4.

After careful consideration, on July 17, 2012 we granted GSK summary judgment and dismissed plaintiff’s claims.

Plaintiff timely appealed on August 15, 2012 and filed her 1925 (b) statement of matters on September 10, 2012. Plaintiff raises the following:

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27 Pa. D. & C.5th 279, Counsel Stack Legal Research, https://law.counselstack.com/opinion/thomas-v-smithkline-beecham-corp-pactcomplphilad-2012.