Sandy Sykes v. United States

507 F. App'x 455
CourtCourt of Appeals for the Sixth Circuit
DecidedNovember 29, 2012
Docket11-4005
StatusUnpublished
Cited by20 cases

This text of 507 F. App'x 455 (Sandy Sykes v. United States) is published on Counsel Stack Legal Research, covering Court of Appeals for the Sixth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Sandy Sykes v. United States, 507 F. App'x 455 (6th Cir. 2012).

Opinion

OPINION

JANE B. STRANCH, Circuit Judge.

Sandy Sykes, appearing pro se,- appeals the district court’s dismissal of all claims filed against the United States, the Department of Veterans Affairs, the University of Cincinnati Medical Center, six individuals, and eight pharmaceutical manufacturers under various statutes and theories, including the Federal Tort Claims Act, 28 U.S.C. §§ 2671-2680; 42 U.S.C. §§ 1983 & 1985; Bivens v. Six Unknown Agents of the Fed. Bureau of Narcotics, 403 U.S. 388, 91 S.Ct. 1999, 29 L.Ed.2d 619 (1971); the Freedom of Information Act, 5 U.S.C. § 552; the Declaration of Helsinki; and Ohio state law. The claims relate to injuries allegedly sustained by Sykes’s brother, David J. Muir, during his participation in clinical drug trials between May 2000 and his death on February 6, 2004. For the reasons stated below, we AFFIRM the district court’s judgment dismissing the claims under Federal Rules of Civil' Procedure 12(b)(1) and 12(b)(6).

I. STANDARD OF REVIEW

We review de novo an order dismissing claims for lack of subject matter jurisdiction under Rule 12(b)(1) and for failure to state a claim under Rule 12(b)(6). McCormick v. Miami Univ., 693 F.3d 654, 658 (6th Cir.2012). In a facial challenge to jurisdiction under Rule 12(b)(1), we construe the allegations of' the complaint as true. Id. In a factual challenge to jurisdiction, we may weigh' evidence to decide whether the factual predicates exist to support subject matter jurisdiction. Id.

To survive a motion to dismiss under Rule 12(b)(6) for failure to state a claim,the complaint must contain “a short and plain statement of the claim showing that the pleader is entitled to relief’ in order to provide fair notice to the defendant of what the claim is and the grounds upon which it rests. Fed.R.Civ.P. 8(a)(2); Bell Atl. Corp. v. Twombly, 550 U.S. 544, 555, 127 S.Ct. 1955, 167 L.Ed.2d 929 (2007). The complaint “must contain more' than conclusions and an unsubstantiated recitation of the necessary elements of-a claim.” McCormick, 693 F.3d at 658. We- assume the factual allegations of the complaint are true and we decide whether the complaint states a plausible claim for relief. See Ashcroft v. Iqbal, 556 U.S. 662, 679, 129 S.Ct. 1937, 173 L.Ed.2d 868 (2009).

When ruling on a motion to dismiss under Rule 12(b)(6), the-court may consider public records and exhibits attached to the complaint without converting the motion to one for summary judgment under Federal Rule of Civil. Procedure 56. Amini v. Oberlin Coll., 259 F.3d 493, 502 (6th Cir.2001). The court may also , consider documents. attached to a motion to dismiss if they are referred to in the complaint and are central to the plaintiffs claim. Id.; Weiner v. Klais & Co., 108 F.3d 86, 89 (6th Cir.1997).

II. FACTUAL. ALLEGATIONS OF THE AMENDED COMPLAINT

The plaintiffs below included Sandy Sykes individually and as administrator of *458 the estate of David J. Muir, Katherine Muir, Margaret Muir, Robert Muir, Eric Muir, and Paul Muir. Represented by-counsel, the plaintiffs initially filed suit on October 4, 2010.

According to the amended complaint filed on December 29, 2010, plaintiffs’ relative, David J. Muir, died on February 6, 2004. An autopsy revealed the cause of natural death was peritonitis due to a perforated sigmoid colon and peritoneal adhe-sions. The autopsy confirmed that Muir suffered from hepatitis C and cirrhosis of the liver.

Before 2000, Muir was severely injured in a house fire. He suffered third-degree burns over sixty-five percent of his body, which required skin grafts, amputation of one hand and amputation of the fingers on the other hand. Because of these injuries, Muir took methadone for continuous pain. He also suffered from severe depression and had attempted suicide. Between 2000 and his death in February 2004, Muir received medical treatment at the Cincinnati Veterans Administration Medical Center and its affiliated locations (VA), and at the University of Cincinnati Medical Center and its affiliated locations (UCMC).

The plaintiffs alleged that, between May 2000 and February 6, 2004, Muir was enrolled in human research studies or clinical drug trials at the VA and UCMC for the treatment of hepatitis C in veterans, and was enrolled to participate in the studies even though he did not qualify due to his pre-existing physical and mental conditions. The plaintiffs further alleged that the studies were administered or supervised by Charles L. Mendenhall, M.D., the study doctor; Gary Roselle, M.D., Medical Director of the VA; and Judith M. Harrer, BS Pharm., Ph.D., the investigational drug pharmacist for the Cincinnati VA Medication Development Research Unit. Although plaintiffs also named as defendants Jeffrey Goldsmith, M.D., Robert Weesner, M.D., and Joseph Morelli, M.D., the amended complaint lacked specific factual allegations concerning these physicians. The plaintiffs alleged that all of the individuals acted within the scope of their employment.

The complaint further alleged that, as a participant in the studies, Muir was subjected to the use of certain medical testing devices and was prescribed certain pharmaceuticals and pharmaceutical test kits contrary to the standards or dosages approved by the U.S. Food and Drug Administration for these products. It alleged that the manufacturers of the pharmaceuticals and devices sponsored the studies and allowed their products to be used for purposes outside FDA-approved indications, and Muir was not advised by the VA, UCMC, or the drug manufacturers about any adverse warnings applicable to the pharmaceuticals that were administered to him. Muir signed at least two consent forms agreeing to participate in studies, but the plaintiffs asserted that the forms were defective in that they did not disclose alternative and safer courses of treatment, did not include proper witness signatures, and did not include adequate descriptions of the compensation or treatment that the VA would provide Muir for any injury he sustained as a result of the studies.

According to the plaintiffs, Muir ingested orally or was injected with approximately ten drugs over a four-year period, including Epogen, Neuprogen, Procrit, Pe-ginterferon, Pegasys, Copegus, Bupriop-ion, Intron A, Rebetol, Rebetron Combination Therapy, and Gabapentin.

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507 F. App'x 455, Counsel Stack Legal Research, https://law.counselstack.com/opinion/sandy-sykes-v-united-states-ca6-2012.