Scanlon v. Secretary of Health & Human Services

114 Fed. Cl. 135, 2013 U.S. Claims LEXIS 2016, 2013 WL 6922296
CourtUnited States Court of Federal Claims
DecidedDecember 17, 2013
DocketNo. 13-219V
StatusPublished
Cited by18 cases

This text of 114 Fed. Cl. 135 (Scanlon v. Secretary of Health & Human Services) is published on Counsel Stack Legal Research, covering United States Court of Federal Claims primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Scanlon v. Secretary of Health & Human Services, 114 Fed. Cl. 135, 2013 U.S. Claims LEXIS 2016, 2013 WL 6922296 (uscfc 2013).

Opinion

OPINION AND ORDER

LETTOW, Judge.

On March 28, 2013, Ms. Ina Scanlon filed a petition for compensation under the National Childhood Vaccine Injury Act of 1986, Pub.L. No. 99-660, § 311,100 Stat. 3743, 3755 (1986) (codified, as amended, at 42 U.S.C. §§ 300aa-l to -34 (“Vaccine Act”)), alleging injury resulting from receipt of the varicella zoster (“shingles”) vaccine. On September 27, 2013, the special master assigned to the case granted the government’s motion to dismiss on the ground that the shingles vaccine is not covered under the Vaccine Act. Ms. Scanlon filed a motion for review of the special master’s decision on September 30, [137]*1372013. A hearing was held on November 15, 2013, and this case is ready for disposition.

BACKGROUND

Ms. Scanlon’s petition recites that she received the shingles vaccine on April 1, 2010 and thereafter suffered a viral infection allegedly caused by the vaccine. Pet. at 1. In March 2010, prior to the vaccination, a physical examination by her family doctor showed she was in good health, with a platelet count of 209,000. Pet. ¶ 2. On May 24, 2010, after noticing severe bruising on her torso, Ms. Scanlon went back to her doctor and discovered that her platelet count had dropped to 6,000. Pet. ¶¶4-5. She was immediately referred to a cancer center where, the next day, Dr. Joseph Spahr diagnosed a virus in Ms. Scanlon’s system that caused the platelet destruction. Pet. ¶ 6. Her platelet levels varied throughout the next year. Pet. ¶ 7. On April 27, 2011, Dr. Shanique R. Palmer of the Mayo Clinic in Rochester, Minnesota concluded that Ms. Scanlon’s problems were caused by the varicella zoster vaccination. Pet. ¶ 8. Ms. Scanlon continues to suffer from inconsistent platelet counts and immune thrombocytopenia,1 characterized by excessive bleeding and dangerous bruising. Pet. ¶¶ 9-11.

Ms. Scanlon filed her petition for compensation in March 2013. In September 2013, the government filed a motion to dismiss for failure to state a claim upon which relief can be granted, pursuant to Rule 12(b)(6) of the Rules of the Court of Federal Claims (“RCFC”). Resp’t’s Mot. to Dismiss (“Resp’t’s Mot.”) at 1, ECF No. 17. The government argued that compensation under the Vaccine Act is only available when a claimant has received a vaccine included in the Vaccine Injury Table (“the Table”), and the shingles vaccine is not so listed. Id. (citing 42 C.F.R. § 100.3). The government further argued that for any vaccine the Secretary of the Department of Health and Human Services (“HHS”) adds to the Vaccine Injury Table, Congress must approve an accompanying excise tax to provide funds for compensation. Id. at 1-2 (citing Omnibus Budget Reconciliation Act of 1993, Pub.L. No. 103-66 § 13632(a)(3), 107 Stat. 312 (1993) (codified as amended at 42 U.S.C. § 300aa-14 note (1993) (Revisions of Vaccine Injury Table)).2 Congress has not enacted an excise tax related to the shingles vaccine. Id. at 2; Hr’g Tr. at 13:20 to 14:6 (Nov. 15, 2013).

The special master agreed with the government that Ms. Scanlon was required to demonstrate that she “received a vaccine set forth in the Vaccine Injury Table” to be able to make a claim for compensation. Scanlon v. Secretary of Health and Human Servs., No. 13-219V, 2013 WL 5755061, at *2 (Fed. Cl.Spee.Mstr. Sept. 27, 2013) (citing 42 U.S.C. § 300aa-ll(c)(l)(a)). Even though “varicella vaccine” appears on the Table, see 42 C.F.R. § 100.3, Table, item X, the special master found that the shingles vaccine could not be considered a covered vaccine and granted the government’s motion to dismiss. Id. at *2-3.

First, the special master was unconvinced by Ms. Scanlon’s assertion that because the chicken pox vaccine and the shingles vaccine both contain live attenuated varicella zoster virus and are linked in the medical literature, both are encompassed by the term “varicella vaccine” on the Vaccine Injury Table. See Scanlon, 2013 WL 5755061, at *2-3. Although the two vaccines are used to prevent two adverse outcomes of an infection from the same virus, the vaccines themselves are distinguishable. Id. at *2. The varicella zoster vaccine (“Zostavax”) and the varicella [138]*138vaccine (“Varivax”) are both manufactured by Merck and contain versions of the same live, attenuated virus, but, upon considering package inserts for each vaccine, the special master determined that they are not an identical vaccine. Id. Varivax contains “a minimum of 1[,]350 plaque-forming units (PFU) of Oka/Merek varicella virus.” Id. (quoting Varivax Package Insert (Frozen) at 6, ¶ 11, available at www.fda.gov/downloads/ biologicsbloodvaccines/vaccines/approved products/UCM142813.pdf). Zostavax, however, contains “a minimum of 19,400 PFU (plaque-forming units) of Oka/Merck strain of VZV [varicella zoster virus].” Id. (quoting Zostavax Package Insert (Frozen) at 8, ¶ 11, available at www.fda.gov/downloads/ biologicsbloodvaecines/vaccines/approved produets/UCM132831.pdf).3 Varivax is “indicated for active immunization for the prevention of varicella in individuals 12 months of age and older,” id. (quoting Varivax Package Insert at 2, ¶ 1), and Zostavax is “indicated for prevention of herpes zoster, (shingles) in individuals 50 years of age and older,” id. (quoting Zostavax Package Insert, at 2, ¶ 1). Zostavax is expressly not indicated for “prevention of primary varicella infection (Chickenpox) and should not be used in children and adolescents.” Id. (quoting Zostavax Package Insert at 8,118.4).

Second, the special master examined the purpose and design of the Vaccine Act in deciding that Zostavax should not be considered a “varicella vaccine” and thus not a covered vaccine. “The Act ‘concerns only the actions of those injured by specified childhood vaccines and the manufacturers of such vaccines____ [F]unding for the program is provided through a tax to be placed on designated childhood vaccines.’” Scanlon, 2013 WL 5755061, at *2 (quoting H.R. Rep. 99-908 at 3 (1986), reprinted in 1986 U.S.C.C.A.N. 6344, 6344). The Secretary of HHS is directed to amend the Vaccine Injury Table only after the Centers for Disease Control and Prevention (“CDC”) recommend a vaccine for “routine administration to children.” Id. at *1 (citing 42 U.S.C. § 300aa-14(e)(2) (relating to vaccines recommended after August 1,1993)). The Zostavax vaccine that Ms. Scanlon received is not indicated for children, unlike the Varivax vaccine. Furthermore, the Omnibus Budget Reconciliation Act of 1993 provides that any amendment to the Vaccine Injury Table only takes effect upon the effective date of an excise tax enacted on the covered vaccine to provide the funds for compensation. Id. (citing 42 U.S.C. § 300aa-14 note (Revisions of Vaccine Injury Table)).

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114 Fed. Cl. 135, 2013 U.S. Claims LEXIS 2016, 2013 WL 6922296, Counsel Stack Legal Research, https://law.counselstack.com/opinion/scanlon-v-secretary-of-health-human-services-uscfc-2013.