Martinez v. TEVA Pharmaceuticals USA, Inc. et al
Filing
64
MEMORANDUM OPINION AND ORDER DENYING 49 MOTION to Dismiss Plaintiff's Complaint, DENYING 22 MOTION TO DISMISS FOR FAILURE TO STATE A CLAIM , DENYING 25 MOTION to Dismiss and Incorporated Memorandum of Law, DENYING 27 MOTION to Dismiss Plaintiff's Complaint and Memorandum of Law In Support. (Signed by Judge Gray H Miller) Parties notified.(rkonieczny, 4)
United States District Court
Southern District of Texas
ENTERED
UNITED STATES DISTRICT COURT
SOUTHERN DISTRICT OF TEXAS
HOUSTON DIVISION
ALBERT MARTINEZ,
Plaintiff,
v.
TEVA PHARMACEUTICALS USA, INC.,
et al.
Defendants.
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July 31, 2018
David J. Bradley, Clerk
CIVIL ACTION H-18-2017
M EMORANDUM O PINION AND O RDER
Pending before the court are motions to dismiss filed by defendants Mayne Pharma Inc.,
individually and as successor to Libertas Pharma, Inc. (Dkt. 22), Sandoz Inc. (Dkt. 25), Teva
Pharmaceuticals USA, Inc. (Dkt. 27), and Taro Phamaceuticals (USA), Inc. (Dkt. 49) (collectively,
“Defendants”).1 Plaintiff Albert Martinez responded. Dkts. 28– 29, 32, 50. Defendants replied.
Dkt. 39, 40, 46, 57. Defendants supplemented their motions with additional authority. Dkts. 56, 61.
Having considered the motions, responses, replies, and applicable law, the court is of the opinion
that the motions should be DENIED.
I. BACKGROUND
This is a pharmaceutical case.2 Dkt. 1 at 2. Defendants manufacture, market, and sell
amiodarone, a generic medication. Id. The United States Food and Drug Administration (“FDA”)
approved amiodarone “only as a treatment of last resort for life-threatening ventricular fibrillation
1
Because Defendants advance the same grounds in support of their individual motions, the
court will address the motions together.
2
For purposes of the motion to dismiss, the court accepts all of Martinez’s allegations as true.
Kaiser Aluminum & Chem. Sales, Inc. v. Avondale Shipyards, Inc., 677 F.2d 1045, 1050 (5th Cir.
1982).
or ventricular tachycardia that could not be controlled with any other FDA approved option.” Id.
“[E]ach consumer [must] receive an FDA-approved Medication guide each time an [a]miodarone
prescription is filled.” Id. at 13. According to Martinez, Defendants “did not validate the efficacy
of their Medication Guide distribution process, and knew or should have known that their
Medication Guides were not reaching patients like [him].” Id. at 10.
Two doctors prescribed amiodarone to Martinez “for a use never approved by the FDA.” Id.
at 2, 9. Martinez filled the prescription and received amiodarone manufactured by each of the four
defendants. Id. at 2. He ingested the drug every day from September 26, 2015, to April 4, 2016.
Id. at 8. He never received a Medication Guide. Id. at 8. If he had received one when he filled his
prescription, “he would have read it, understood the risks of [a]miodarone [as well as] the approved
uses of [a]miodranone, and would not have taken [it].” Id.
Martinez alleges he did not receive a Medication Guide because Defendants negligently
designed, implemented, and validated a process for distributing those guides. Id. at 9. According
to Martinez, Defendants “failed to take reasonable measures to provide [him] or his dispenser with
the Medication Guides for [a]miodarone as required by federal and parallel state law” each time he
filled his prescription.3 Id. at 9, 15. He alleges that amiodarone proximately caused his injuries,
including: pulmonary toxicity, Parkinson’s disease, visual disturbances, vocal disturbances, and
muscle weakness. Id. at 2. Martinez sued Defendants to recover in negligence and gross
negligence. Id.
3
According to Martinez, “[t]he overarching intent of federal prescription drug regulation and
parallel Texas state law requirements is protecting patients from drugs that are ineffective, unsafe[,]
or both . . . and ensuring that . . . consumers are provided required information before each . . .
decides to . . . use a drug.” Dkt. 1 at 2. He also asserts that “[t]his is . . . the basis for the duty the
states impose on drug makers under both their common law and drug regulatory programs.” Id.
2
II. LEGAL STANDARD
“Federal Rule of Civil Procedure 8(a)(2) requires only ‘a short and plain statement of the
claim showing that the pleader is entitled to relief,’ in order to ‘give the defendant fair notice of what
the . . . claim is and the grounds upon which it rests.’” Bell Atl. Corp. v. Twombly, 550 U.S. 544,
570, 127 S. Ct. 1955 (2007) (internal quotations omitted). In considering a motion to dismiss under
Rule 12(b)(6), courts accept the factual allegations contained in the complaint as true. Kaiser, 677
F.2d at 1050. The court does not look beyond the face of the pleadings to determine whether the
plaintiff has stated a claim under Rule 12(b)(6). Spivey v. Robertson, 197 F.3d 772, 774 (5th Cir.
1999). The complaint “does not need detailed factual allegations, [but] a plaintiff’s obligation to
provide the ‘grounds’ of his ‘entitle[ment] to relief’ requires more than labels and conclusions, and
a formulaic recitation of the elements of a cause of action will not do.” Twombly, 550 U.S. at 556
(internal citations omitted). The factual allegations must be: (1) enough to “raise a right to relief
above the speculative level”; and (2) plausible—enough to raise a reasonable expectation that
discovery will reveal further supporting evidence. Id.
III. ANALYSIS
Defendants move to dismiss Martinez’s claims under Rule 12(b)(6). Defendants attack
Martinez’s claims as: (1) preempted; (2) barred by the learned intermediary doctrine; and (3) failing
to allege sufficient facts. Because each of these grounds fail, the court DENIES each of the motions.
A.
Preemption
Defendants argue that Martinez’s claims are impliedly preempted by federal law. See, e.g.,
Dkt. 22 at 4–6; Dkt. 25 at 6, 10; Dkt. 27 at 15–27; Dkt. 49 at 18. They argue that Martinez’s claims
impermissibly intrude on the FDA’s exclusive authority to enforce its medication guide regulation
because his claims arise solely by virtue of those regulations. See, e.g., Dkt. 22 at 4–6 (relying on
3
Buckman Co. v. Pls.’ Legal Comm., 531 U.S. 341, 352, 121 S.Ct. 1012 (2001)); Dkt. 49 at 18
(relying on Perdue v. Wyeth Pharms., Inc., 209 F. Supp. 3d 846, 850–54 (E.D.N.C. 2016)).
Martinez relies on two recent Texas federal district court cases to argue that his claims are
not preempted: Monk v. Wyeth Pharmaceuticals, Inc., No. 5-16-cv-1273-XR, 2017 WL 2063008,
at *1 (W.D. Tex. May 11, 2017) (Rodriguez, J.), and Mitchell v. Wyeth Pharmaceuticals, Inc., No.
1:16-cv-574-LY, 2017 WL 7361750, at *1 (W.D. Tex. Feb. 9, 2017) (Yeakel, J.) (adopting
magistrate judge’s recommendation). See Dkt. 28 at 7–11. Both of those amiodarone cases analyzed
and rejected arguments that are almost identical to those the Defendants advance here. Compare
Monk, 2017 WL 2063008, at *1, and Mitchell, 2017 WL 7361750, at *1, with Dkt. 22 at 4–6, and
Dkt. 25 at 6, 10, and Dkt. 27 at 15–27, and Dkt. 49 at 18. And both cases relied on the Fifth
Circuit’s decision in Eckhardt v. Qualitest Pharmaceuticals, Incorporated, 751 F.3d 674, 679 (5th
Cir. 2014). See Monk, 2017 WL 2063008, at *2; see also Mitchell, 2017 WL 7361750, at *5–7.
Monk determined that an estate’s negligence and gross negligence claims were not
preempted. 2017 WL 2063008, at *4. Like Martinez, the Monk doctors prescribed amiodarone for
an off-label use and the decedent-patient never received a Medication Guide. See id. at *1. And,
just like Martinez, the Monk patient “did not know . . . the risks of taking amiodarone, the
Medication Guide would have given him this information, and he would not have taken amiodarone
had he been fully informed.” Id.
Monk analyzed Buckman and Eckhardt to determine that the estate’s claims were not
preempted. Id. Monk reasoned that: (1) Buckman does not preempt parallel claims;4 and
4
Monk explained:
Buckman dealt with ‘fraud-on-the-FDA’ claims involving a medical
device manufacturer allegedly using fraudulent tactics to obtain FDA
4
(2) Eckhardt “found that claims for failing to provide FDA approved warnings (like the Plaintiff’s
here) are indeed parallel claims.”5 Id. at *4, *6. Monk cited Mitchell and two other district court
cases as following Eckhardt.6 Id. at *5 (citing Mitchell, 2017 WL 7361750, at *5–7, and Priest v.
approval for a device and plaintiffs subsequently bringing private
causes of action against the manufacturer for its misrepresentations
to the FDA. Recognizing that private, state law causes of action for
fraud-on-the-FDA conflict with federal law because they skewed ‘a
somewhat delicate balance of statutory objectives’ covered by the
FDA, the Supreme Court found that these claims were preempted.
The broader lesson from Buckman . . . is that state law claims that
exist ‘solely by virute’ of the FDCA requirements are preempted.
[. . .]
Crucially, however, the Buckman court distinguished preempted
‘fraud-on-the-agency’ claims from those based on ‘traditional state
tort law principles of the duty of care,’ recognizing that ‘certain statelaw causes of actions that parallel federal safety requirements are not
preempted.’ This distinction is logical . . . the reason for preempting
‘fraud-on-the-agency claims is primarily to protect the ‘somewhat
delicate balance of statutory objectives’ that could be skewed by
interference from private enforcement but pre-existing state law tort
principles alone do not implicate the same concern.
Id. (discussing Buckman, 531 U.S. at 352).
5
Monk explained that the Eckhardt plaintiff sued generic drug manufacturers:
for fail[ing] to provide the plaintiff or his physician with any FDAapproved warnings. Ultimately, the Fifth Circuit affirmed the district
court’s dismissal of these claims because the plaintiff did not make
adequate factual allegations. Before doing so, however, the court
indicated that because ‘failing to provide FDA-approved warnings
would be a violation of both state and federal law, this is a parallel
claim that is not preempted.’
2017 WL 2063008, at *5 (discussing Eckhardt, 751 F.3d at 679) (emphasis added). Defendants
argue that “Eckhardt has no bearing on this case . . . [because] plaintiff was alleging that his
prescribing physician was not provided with adequate warnings.” See, e.g., Dkt. 27 at 21. This
argument fails because Defendants disregard the Eckhardt estate also alleged that the patient did not
receive adequate warnings. See 751 F.3d at 679.
6
Mitchell “involv[ed] similar allegations based on generic amiodarone manufacturers’ failure
to provide Medication Guides.” 2017 WL 2063008, at *6 (discussing Mitchell, 2017 WL 7361750,
5
Sandoz Inc., 1-15-cv-822-ML-LY, 2017 WL 8896188, at *2 (W.D. Tex. Dec. 28, 2017) (adopting
magistrate judge’s report and recommendation), and Rusk v. Wyeth-Ayerherst Labs., No. 1-14-cv549-LY, 2015 WL 11050913, at *1 (W.D. Tex. Oct. 26, 2015) (Yeakel, J.) (same)). The Monk court
explained that it took “the simple step of connecting the rule of Buckman with the finding of
Eckhardt.” Id. at *7.
Defendants repeat the challenges the Monk defendants advanced against Eckhardt. Compare
id., with Dkt. 27 at 20, and Dkt. 57 at 5–8. But just as Monk explained: “Defendants ignore . . . that
regardless of the explanation in Eckhardt, this Court is bound by Fifth Circuit precedent, which
expressly recognizes that a claim for failure to provide FDA-approved warnings alleges a violation
of both [Texas] and federal law and that such a claim is a parallel claim that is not preempted.”7
2017 WL 2063008, at *6 (citing Eckhardt, 751 F.3d at 679) (internal quotations omitted); cf. Dkt.
63 (supplementing with McDaniel v. Upsher-Smith Labs., Inc., 893 F.3d 941, 942 (6th Cir. 2018));
Dkt. 56 (supplementing with Small v. Amgen, Inc., 723 F. App’x 722, 723 (11th Cir. 2018)). To the
extent that Defendants ask this court to disregard Eckhardt, the court declines.
at *8). Mitchell determined that “to the extent [plaintiff] seeks to allege that Defendants failed to
comply with their obligation to supply distributors with the FDA-required Medication Guides, and
this failure proximately caused [the decedent] to take amiodarone without knowledge of the FDAapproved warnings, such a claim would survive federal preemption under Eckhardt’s reasoning.”
Id.
7
Defendants assert that other Fifth Circuit cases require this court to conclude that Martinez’s
claims are preempted. See, e.g., Dkt. 27 at 17 (citing Morris v. Pliva, Inc., 713 F.3d 774, 777 (5th
Cir. 2013) (per curiam), and Estes v. Lanx, Inc., 660 F. App’x 260, 262 (5th Cir. 2016) (per curiam)).
Defendants argue that Morris extends to the distribution of FDA-mandated medication guides. Dkt.
27 at 17 (citing Morris, 713 F.3d at 777). Defendants urge the court to assume that the Fifth Circuit
would treat federal labeling obligations as equivalent to FDA-mandated Medication Guides. Id. at
18. The court will not make that leap without further guidance from the Fifth Circuit. Defendants
also argue that under Estes, Martinez has no private right of action. See Dkt. 27 at 15.
Estes analyzed “fraud-on-the-FDA” claims. 660 F. App’x at 621. That is not what Martinez alleges
here. See Dkt. 1 at 2.
6
B.
Learned intermediary doctrine
Defendants argue that the Texas’s learned intermediary doctrine bars Martinez’s claims. See
Dkt. 22 at 7; Dkt. 27 at 9; Dkt. 40 at 7; Dkt. 49 at 7–8, 15–17. “Under Texas law, to prevail on a
negligence cause of action, the plaintiff must prove the existence of a legal duty, a breach of that
duty, and damages proximately caused by the breach.” Fret v. Melton Truck Lines, Inc., 708 F.
App’x 824, 827 (5th Cir. 2017) (internal citations omitted). Under the learned intermediary doctrine,
“the manufacturer of a pharmaceutical product satisfies its duty to warn the end user of its product’s
potential risks by providing an adequate warning to a ‘learned intermediary,’ who then assumes the
duty to pass on the necessary warnings to the end user.” Centocor, Inc. v. Hamilton, 372 S.W.3d
140, 158 (Tex. 2012).
Defendants argue that the learned intermediary doctrine precludes the existence of duty and
thus bars Martinez’s claims. See Dkt. 22 at 7; Dkt. 27 at 9; Dkt. 40 at 7; Dkt. 49 at 7–8, 15–17.
Martinez disagrees by relying on Centocor. Dkt. 28 at 12–13 (citing 372 S.W.3d at 158); Dkt. 32
at 6 (same).
Monk determined that the learned intermediary doctrine did not bar the plaintiff’s claims.
2017 WL 2063008, at *7. The Monk court explained that “[w]here warnings to a learned
intermediary are adequate, a drug manufacturer fulfills its duty to warn end users of its products
under Texas law, but this result occurs only if the drug manufacturer provided adequate warnings.”
Id. (learned intermediary doctrine did not bar plaintiff’s claims). In that case, the “[p]laintiff . . . pled
that Defendants failed to provide adequate warnings of the danger of their products, and under Texas
law, this sufficiently states a claim.” Id.
Just as in Monk, Martinez has pled that Defendants did not provide adequate warnings of the
risks of taking amiodarone by failing to ensure that Medication Guides reached him and patients like
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him. Compare id., with Dkt. 1 at 2, 8–9. Accordingly, the learned intermediary doctrine does not
bar Martinez’s claims at this stage. Cf. Monk, 2017 WL 2063008, at *7 (“Whether those warnings
were in fact adequate—such that the learned intermediary doctrine would shield Defendants from
liability—can be considered at the summary judgment phase after the parties have conduct discovery
on the issue.”).
C.
Pleading deficiencies8
Defendants argue that Martinez fails to allege sufficient facts to survive Rule 8(b)(2). See,
e.g., Dkt. 22 at 3; Dkt. 49 at 19; Dkt. 57 at 12. Because Martinez’s allegations raise a right to relief
above a speculative level, the court disagrees. See Twombly, 550 U.S. at 555; see also Kaiser, 677
F.2d at 1050. Namely, Martinez alleges that: (1) the Medication Guide gave information about the
risks of taking amiodarone; (2) he never received a Medication Guide; (3) had he received one, he
would not have taken amiodarone; and (4) he suffered injuries because he took amiodarone. See
Dkt. 1 at 2, 8–9. He also alleges that Defendants knew or should have known that patients like him:
(1) were receiving off-label prescriptions; and (2) were not receiving Medication Guides. Id. And
he alleges that Defendants did not ensure that pharmacies had enough Medication Guides to give to
patients like Martinez. Id. These allegations satisfy Rule 8(a)(2).
IV. CONCLUSION
Defendants’ motions to dismiss (Dkts. 22, 25, 27, 49) are DENIED.
Signed at Houston, Texas on July 31, 2018.
___________________________________
Gray H. Miller
United States District Judge
8
Defendants argue that Martinez impermissibly combines allegations about the manufacturers
together. See, e.g., Dkt. 25 at 6, 17; Dkt. 49 at 21. “The fact that plaintiff accuses all . . . defendants
of the same wrongdoings is not a basis for dismissal.” Monk, 2017 WL 2063008, at *9.
8
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