United States ex rel. Kroening v. Forest Pharmaceuticals, Inc.

155 F. Supp. 3d 882, 2016 U.S. Dist. LEXIS 3509, 2016 WL 75066
CourtDistrict Court, E.D. Wisconsin
DecidedJanuary 6, 2016
DocketCase No. 12-CV-366
StatusPublished
Cited by7 cases

This text of 155 F. Supp. 3d 882 (United States ex rel. Kroening v. Forest Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. Wisconsin primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States ex rel. Kroening v. Forest Pharmaceuticals, Inc., 155 F. Supp. 3d 882, 2016 U.S. Dist. LEXIS 3509, 2016 WL 75066 (E.D. Wis. 2016).

Opinion

DECISION AND ORDER

WILLIAM E. DUFFIN, UNITED STATES Magistrate Judge

I. Procedural History

On April 18, 2012, relator Kurt Kroening filed the present action on behalf of the United States, 30 states, and the District of Columbia under the False Claims Act and similar state statutes. After a lengthy period for investigation, the United States filed notice on January 31, 2014, that it was not intervening. (ECF No. 23.) The case was unsealed (ECF No. 24), and on June 13, 2014, Kroening filed an amended complaint on behalf of the United States, the District of Columbia, and twenty-eight states (ECF No. 34). After the court approved several stipulations to extend the deadline for defendants Forest Pharmaceuticals, Inc. and Forest Laboratories, Inc. (herein collectively “Forest”) to respond to the amended complaint (ECF Nos. 39, 40, 43, 44, 45, 47), on March 16, 2015, Forest filed a motion to dismiss (ECF No. 50). Briefing on the motion was completed on May 11, 2015. All parties have consented to have this court enter final judgment in this matter. (ECF Nos. 38, 41, 42.)

II. Allegations in the Amended Complaint

In June of 2007, Kroening began working for Forest Pharmaceuticals, Inc. as a pharmaceutical sales representative. (ECF No. 34, ¶¶ 3,19.) For several years prior to Kroening’s employment and continuing until at least the filing of the amended complaint (ECF No. 34, ¶ 19), Forest maintained a “Speakers Bureau” program whereby it would pay prescribers of Forest drugs for speaking at presentations. Speakers received not only direct compensation of between $1,000 and $1,750 per presentation (ECF No. 34, ¶ 48) but also lavish meals, drinks (ECF No. 34, ¶¶ 43, 49), and travel expenses (ECF No. 34, ¶¶ 29, 58). The purpose of the Speakers Bureau was not education but to incentivize prescribers to write prescriptions for Forest drugs. (ECF No. 34, ¶ 30.) Educational content and even actual attendance were not relevant to Forest. (ECF No. 34, ¶¶ 38, 46, 50.) Sometimes prescri-bers were paid a speaker’s fee even though they did not present a speech or make a presentation. (ECF No. 34, ¶¶ 53, 59.) When a presentation did occur, it was generally only about 5 to 10 minutes in length and not necessarily related to any Forest drug. (ECF No. 34, ¶ 59.) After Forest changed its policies in 2010 to require two providers at a presentation, attendance records were often falsified in an effort to provide evidence that the attendance requirement was met. (ECF No. 34, ¶¶ 28, 50, 54, 55, 56, 58.)

Physicians were chosen to give presentations “based on their actual and potential prescription writing volume.” (ECF No. 34, ¶ 31.) Also relevant was whether the physician had a high number of Medicare and/or Medicaid patients. (ECF No. 34, ¶ 41.) Sales representatives actively tracked the prescriptions of speakers to ensure an adequate “return on investment.” (ECF No. 34, ¶¶ 32, 34, 60.) If a provider in the Speakers Bureau did not increase or maintain his prescription vol[886]*886ume for Forest drugs, he was dropped from the program. (ECF No. 34, ¶¶ 28, 35, 45.)

Kroening contends that the speaking fees and related compensation constituted unlawful kickbacks. As a result of the “kickbacks, misrepresentations and submissions of non-reimbursable claims” described in the amended complaint (ECF No. 34, ¶¶ 64, 69, 74), Forest “knowingly-presented or caused to be presented false or fraudulent claims for the improper payment or approval of prescriptions of Forest drugs” (ECF No. 34, ¶ 64 (citing 31 U.S.C. § 3729(a)(1)(A))), “knowingly made, used, or caused to be made or used false records or statements material to a false or fraudulent claim for the improper payment or approval of prescriptions of Forest drugs” (ECF No. 34, ¶69 (citing 31 U.S.C. § 3729(a)(1)(B))), and “knowingly conspired to commit violations of the False Claims Act for the improper payment or approval of prescriptions of all of its drugs for which it included providers in its Speakers Bureau” (ECF No. 34, ¶ 74 (citing 31 Ú.S.C. § 3729(a)(1)(C))).

III. Motion to Dismiss Standard

“To survive a motion to dismiss under Rule 12(b)(6), a complaint must provide enough factual information to ‘state a claim to relief that is plausible on its face’ and ‘raise a right to relief above the speculative level.’ ” Thulin v. Shopko Stores Operating Co., LLC, 771 F.3d 994, 997 (7th Cir.2014) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 555, 570, 127 S.Ct. 1955, 167 L.Ed.2d 929 (2007)). The court not only considers the context of the ease but also may draw upon its own judicial experience and common sense when assessing whether a complaint states a claim upon which relief may be granted. Id. (quoting Ashcroft v. Iqbal, 556 U.S. 662, 679, 129 S.Ct. 1937, 173 L.Ed.2d 868 (2009)). Well-pleaded facts are accepted, as true and construed in the light most favorable to the plaintiff. Id. (citing Camasta v. Jos. A. Bank Clothiers, Inc., 761 F.3d 732, 736 (7th Cir.2014)). Because this action arises under the False Claims Act, 31 U.S.C. § 3729 et seq., the amended complaint must satisfy the heightened pleading requirements of Fed. R. Civ. P. 9(b). Id. at 998 (citing United States ex rel. Gross v. AIDS Research Alliance-Chicago, 415 F.3d 601, 604 (7th Cir.2005)).

IV. Analysis

The False Claims Act (FCA) is “the primary vehicle by the Government for recouping losses suffered through fraud.” 31 U.S.C. § 3729 et seq. The Attorney General may bring actions under the FCA directly in the name of the United States. 31 U.S.C. § 3730(a). Alternatively, a private person known as a “relator” may bring a qui tarn action “in the name of the Government.” 31 U.S.C. § 3730(b). If the qui tam action results in the recovery of money for the government, the relator shares in the award. See 31 U.S.C. § 3730(d).

The FCA imposes civil liability on any person who “knowingly presents, or causes to be presented” to the United States or its representatives “a false or fraudulent claim for payment or approval,” 31 U.S.C. § 3729(a)(1)(A), or “knowingly makes, uses, or causes to be made or used, a false record or statement material to a false or fraudulent claim,” 31 U.S.C. § 3729(a)(1)(B).

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155 F. Supp. 3d 882, 2016 U.S. Dist. LEXIS 3509, 2016 WL 75066, Counsel Stack Legal Research, https://law.counselstack.com/opinion/united-states-ex-rel-kroening-v-forest-pharmaceuticals-inc-wied-2016.