ORDER GRANTING PLAINTIFFS’ MOTION FOR CLASS CERTIFICATION
This case involves a claim to recover economic damages resulting from the purchase of the prescription drug Duract, which has been taken off the market due its risk of causing liver damage. Plaintiffs bring claims on their own behalf and on behalf of a class of purchasers of Duract. Now before the Court is Plaintiffs’ Motion for Class Certification. For the reasons stated below, Plaintiffs’ Motion is GRANTED.
I. BACKGROUND
Plaintiff Rivera purchased Duract, a nonsterodial anti-inflammatory drug used for the management of pain. Plaintiff Arkansas Carpenters Health and Welfare Fund (“Arkansas Fund”) is a health plan which paid for some or all of Plaintiff Rivera’s Duract expenses. Defendants introduced Duract in 1997, but withdrew the drug from the market some eleven months later following reports of liver damage among its users. Plaintiffs allege that prior to introducing Duract, Defendants were aware of the life threatening side-effects associated with it, even in people who use the medicine for less than ten days. Plaintiffs further contend that Defendants did not adequately disclose such side-effects to patients and physicians.
Plaintiffs seek to recover economic damages resulting from the purchase of Duract. They assert claims for: (1) violations of the Texas Deceptive Trade Practices Act (“DTPA”), TexBus. & Com.Code Ann. § 17.46 et seq. (Vernon Supp.1998); (2) breach of the implied warranty of merchantability under TexBus. & Com.Codb Ann. § 2.314(a) (Vernon 1994); and (3) unjust enrichment.
Pursuant to Federal Rule of Civil Procedure 23, Plaintiffs seek to certify a nationwide class of purchasers of Duract. The proposed class includes “individual consumers who purchased the prescription drug Duract, marketed and sold by Defendants, and who have not manifested signs of physical injury resulting from Defendants’ conduct, health insurance companies, managed care organizations, self-funded health benefit plans, and other private entities that have provided prescription drug coverage and expended funds for Duract under private plans
II. STANDARD FOR CLASS CERTIFICATION
The party seeking class certification has the burden of showing that the requirements for a class action have been met. See, e.g., Applewhite v. Reichhold Chem., Inc.,
In the instant case, Defendants claim that Plaintiffs lack standing to prosecute the action on behalf of the class. In addition, Defendants contest the class certification requirements of adequate representation, predominance, and superiority. The Court nevertheless finds that the requirements for class certification have been met. Consequently, Plaintiffs’ Motion for Class Certification is GRANTED.
III. ANALYSIS
A. Standing
As a preliminary matter, the Court considers Defendants’ contention that Plaintiffs lack standing to prosecute the class action. Defendants argue that Plaintiffs lack standing because they did not suffer physical injury from the use of Duract. As the argument was addressed in Defendants’ Motion to Dismiss, which the Court denied in a previous order, Defendants cannot relitigate the issue here. See Eisen v. Carlisle & Jacquelin,
B. Rule 28(a) Prerequisites
1. Numerosity
The first prerequisite to a class action under Rule 23(a) is that “the class is so numerous that joinder of all members of the class is impractical.” There is no threshold size for a class action, and the issue of numerosity must be determined on a case by case basis. See 7A Challes Alan Wright, Arthur R. Miller and Mary Kay Kane, Federal Practice and Procedure § 1762 (1986). The burden of showing impracticability rests with the class representative seeking certification. The class representative need not determine exactly how many members the class will contain, but on the other hand, should not engage in mere speculation as to the size of a class. See Marcial v. Coronet Ins. Co.,
In this case, potential class members number in the tens of thousands. Furthermore, the class contains members from across the nation. Thus, it is apparent that joinder would be impractical. See Mullen v. Treasure Chest Casino, LLC,
2. Commonality
The second prerequisite to a class action under rule 23(a) is that “there are questions of law or fact common to the class.” The test is not demanding and only requires that “there is at least one issue, the resolution of which will affect all or a significant number of the putative class members.” Mullen,
Common questions of law and fact in this case include: 1) whether Defendants engaged in deceptive marketing; 2) whether Defendants breached any express or implied warranties; 3) whether Defendants’ warnings were adequate; 4) whether Defendants failed to disclose information regarding the safety of the product; 5) whether the product was in fact safe; 6) whether Defendants were aware of the risk when they introduced the product; and 7) whether Defendants were unjustly enriched. These questions, when answered for one class member, are answered for all. Thus, the commonality requirement is met.
3. Typicality
The third prerequisite to a class action under rule 23(a) is that “the claims or defenses of the representative parties are typical of the claims and defenses of the class.” Like the commonality requirement, the threshold for typicality is not high. See Mullen,
In this case, the named Plaintiffs appear to be typical purchasers of Duract. There is no indication that they will be preoccupied with defenses applicable only to themselves. Thus, the typicality requirement is met.
4. Adequate Representation
The fourth prerequisite to a class action under rule 23(a) is that “the representative parties will fairly and adequately protect the interest of the class.” The test focuses upon the adequacy of both the class representative and the class counsel. See Wright et al., supra § 1765.
Because Plaintiffs’ claims are typical of the claims of the members of the proposed class, the class representatives’ interests are
Defendants argue that the class representatives are not adequate because the consumers and third-party payers may have a potential conflict. They claim that in the case of a settlement, consumers and third-party payers will have a conflict regarding priority of repayment. Thus, Defendants argue that Plaintiffs’ counsel cannot represent both groups. In the unlikely event that a conflict does occur over allocation of damages or settlement funds, however, the Court can divide the class into two subclasses consisting of consumers and insurers, appointing separate counsel for each. See Fed.R.Civ.Pro. 23(c)(4)(A) (allowing the Court to create subclasses); Payne v. Travenol Lab., Inc.,
C. Rule 23(b)(3) Requirements
In addition to meeting the prerequisites listed in Rule 23(a), the Plaintiff must meet at least one of the requirements of Rule 23(b). In this case, the Plaintiffs rely on Rule 23(b)(3) which allows a District Court to maintain a class action if “the court finds that the questions of law or fact common to the members of the class predominate over any questions affecting only individual members, and that a class action is superior to other available methods for the fair and efficient adjudication of the controversy.”
1. Predominance
Defendants argue that individual issues of reliance and causation predominate over common issues. Individual issues of reliance will defeat the predominance requirement. See Castano,
Defendants contend that the learned intermediary doctrine creates the necessity of an individualized treatment. Under the learned intermediary doctrine, the manufacturer of a prescription drug discharges his duty to warn by supplying an adequate warning to the prescribing physician. See Hurley v. Lederle Labs.,
Defendants also contend that variations in state law defeat predominance. Variations in state law may swamp common issues in certain cases. See Castano,
Plaintiffs respond that in a recent, similar nationwide class action, the same Defendants as in this ease were able to fashion a settlement involving claims of injury and economic loss for all class members. They attach to their brief the Official Court Notice of Nationwide Diet Drug Class Action Settlement. That case, however, involved a settlement-only class certification. See In re Diet Drugs Prod. Liab. Litig.,
Nevertheless, under Federal Rule of Civil Procedure 23(c)(1), a Court must determine whether a class action is maintainable “as soon as practicable.” Moreover, under Rule 23(c)(4)(A), the Court may divide a class into subclasses. The Court can overcome difficulties created by variations in state law through the judicious use of subclasses. See Spence,
2. Superiority
In addition to proving predominance, Plaintiffs must also show that a class action “is superior to other available methods for the fair and efficient adjudication of the controversy.” Factors for the Court to consider include: “(A) the interest of members of the class in individually controlling the prosecution or defense of separate actions; (B) the extent and nature of any litigation concerning the controversy already commenced by or against members of the class; (C) the desirability or undesirability of concentrating the litigation of the claims in the particular forum; and (D) the difficulties likely to be encountered in the management of a class action.” Fed.R.Civ.P. 23(b)(3).
Plaintiffs argue that not only is a class action the superior method for adjudicating this controversy, it is the only method. Because the individual claims involved are relatively small, absent a class action it would be economically unfeasible for class members to prosecute individual claims. See Shaw,
Defendants argue that the class action would be unmanageable. They claim that the Court would have to decide for each Plaintiff: (1) who prescribed the drug; (2) when the drug was prescribed; (3) whether the prescriber read the drug labeling; (4) whether the prescriber was aware from any source, of the risks of the drug; (5) whether the drug prescriber would have still prescribed the drug had he known what he knows now; (6) what Plaintiff paid; and (7) whether the Plaintiff has been reimbursed by his insurance company. Points one through five go to the learned intermediary doctrine, which the Court has already held has no bearing in this case for economic damages. The Court might also note with regard to point five, being that the Duract has been taken off the market because of its health risks, it is incontestable that no physician would prescribe Duract now. As to point six, although what various Plaintiffs paid for Duract may differ, there is obviously no requirement that all class members have identical damages. See Shaw,
Finally, Defendants argue that the class definition is flawed because it includes both the consumers and their insurers. Defendants argue that this will lead to a double recovery. This argument is flawed and contradicted by Defendants’ observation that reimbursement amounts will have to be determined. Both third-party payers and consumers are members of the class because in most cases the third-party payers paid for some, but not all, of the consumer’s Duract expenses. This was the case of the named Plaintiffs. Rather than creating a double recovery, having all these parties together prevents a double recovery.
Taking the 23(b)(3) factors in turn, (A) as damages are small, members of the class do not have an interest in individually controlling the prosecution or defense of separate actions, (B) there is no indication that litigation concerning the controversy has already been commenced by members of the class, (C) because of economies of scale, it is desirable to concentrate the litigation of the
D. Additional Time
Defendants argue in the alternative that class certification is premature and that they should be granted more time to conduct discovery on class certification issues. Defendants’ Response to Plaintiffs’ Motion for Class Certification was filed on October 6, 2000 and the original complaint bringing this class action was filed on June 13, 2000. Thus, Defendants had almost four months to pursue discovery on class certification before responding. In addition, the items for which Defendants seek additional discovery, whether Plaintiff Arkansas Fund is a consumer within the meaning of the DTPA, the amounts the named Plaintiffs paid for Duract, the number of prescriptions paid for by the named fund, and the nature of the Named Fund’s contractual obligations to its insureds, are relevant only to the merits of the case and thus have no bearing on the issue of class certification. See Eisen,
TV. CONCLUSION
For the reasons stated above, the Court CERTIFIES this class under Federal Rule of Civil Procedure 23(b)(3). Defendants’ request that the Court defer its ruling pending additional class discovery is DENIED. The class includes: individual consumers who purchased the prescription drug Duract, marketed and sold by Defendants, and who have not manifested signs of physical injury resulting from Defendants’ conduct, health insurance companies, managed care organizations, self-funded health benefit plans, and other private entities that have provided prescription drug coverage and expended funds for Duract under private plans with individuals or their employers. Excluded from the class are purchasers or users of Duract who have manifested physical injury allegedly as a result of taking said drug and the officers, directors or immediate family of any officer or director of Defendants. Plaintiffs are to submit a workable subclass plan, or a detailed analysis showing why one is not needed, within sixty days.
IT IS SO ORDERED.
Notes
. By the stipulation of the parties, Plaintiffs have voluntarily dismissed their claims for breach of an implied warranty for fitness for a particular purpose and an alleged private right of action under the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. §§ 352, 331. Also, on July 25, 2000, in their First Amended Complaint, Plaintiffs added a claim for violation of the Racketeer Influenced and Corrupt Organizations Act (RICO), 18 U.S.C. § 1961 et seq. Plaintiffs’ Second Amended Complaint, however, omits this RICO allegation.
