Longmire v. Upjohn Co.

686 F. Supp. 659, 1988 U.S. Dist. LEXIS 6145, 1988 WL 66070
CourtDistrict Court, S.D. Ohio
DecidedJune 24, 1988
DocketC-1-85-1808
StatusPublished
Cited by1 cases

This text of 686 F. Supp. 659 (Longmire v. Upjohn Co.) is published on Counsel Stack Legal Research, covering District Court, S.D. Ohio primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Longmire v. Upjohn Co., 686 F. Supp. 659, 1988 U.S. Dist. LEXIS 6145, 1988 WL 66070 (S.D. Ohio 1988).

Opinion

*660 ORDER GRANTING MOTION FOR SUMMARY JUDGMENT OF DEFENDANT THE UPJOHN COMPANY

SPIEGEL, District Judge.

This matter came on for consideration of the motion for summary judgment of defendant Upjohn Company (doc. 27), plaintiff’s memorandum in opposition (doc. 29), together with affidavits (docs. 30, 31, 32), and defendant’s supplemental memorandum (doc. 33), and reply to plaintiff’s memorandum (doc. 34).

This action was commenced on November 6, 1985 against the Upjohn Company (Upjohn) alleging that plaintiff was prescribed depo-Provera, a pharmaceutical product manufactured by Upjohn which caused her numerous medical problems. According to the defendant at the time plaintiff’s gynocologist prescribed depoProvera for her, it was a prescription pharmaceutical product produced and marketed by Upjohn in the United States for use in the treatment of habitual and threatened abortion and endometriosis. Plaintiff claims she was prescribed depo-Provera as a contraceptive but defendant contends that Upjohn never recommended manufactured, and produced, sold, marketed or promoted or otherwise placed depo-Provera in distribution in United States for use as a contraceptive.

Be that as it may, plaintiff admits first receiving injections of depo-Provera after the birth of her first child in 1965 which injections continued until April of 1967. She again received injections of depo-Provera from December 1969 until September of 1970. She has not taken them since that time. Plaintiff admits being told by her gynocologist, Dr. Schwarz in 1970 that he had given her too much depo-Provera and that this over prescription may cause her problems. Plaintiff later consulted with two other gynocologists, Dr. Mationlionnes and Dr. Scharinavas, who advised her that her medical problems may be related to depo-Provera.

In January 1983 an article appeared in the Cleveland Plain Dealer in which plaintiff was the subject and in which she blamed her medical problems on depo-Provera. The interview was arranged by representatives of the National Womens Health Network, an organization which was spearheading the dissemination of information about depo-Provera. Plaintiff first learned of the Network through an article which described the different symptoms associated with depo-Provera and requested that women who had taken the drug contact the Network. Plaintiff did so in 1981 and informed the Network that she had taken depo-Provera and had experienced all of the symptoms listed in the article. The director of the Network asked her if she would be willing to share her story with a newspaper reporter, which she agreed to do, and the interview appeared in the Cleveland Plain Dealer on January 8, 1983. More than two years before the filing of the instant law suit.

This is a diversity action removed to the Federal Court by Upjohn. Under Erie v. Tompkins, 304 U.S. 64, 58 S.Ct. 817, 82 L.Ed. 1188 (1938) we look to the law of Ohio and apply the Ohio two-year statute of limitations to plaintiff’s bodily injuries, § 2305.10 Ohio Rev. Code. The Supreme Court of Ohio in O’Stricker v. Jim Walter Corp., 4 Ohio St.3d 84, 447 N.E.2d 727 (1983) has adopted the following discovery rule for accrual of causes of action under § 2305.10 Ohio Rev. Code:

When an injury does not manifest itself immediately, the cause of action arises upon the date on which the plaintiff is informed by competent medical authority that he has been injured, or upon the date on which, by the exercise of reasonable diligence, he should have become aware that he had been injured, whichever date occurs first.

Defendant argues that under either prong of the above discovery rule, plaintiff’s cause of action accrued more than two years before her filing of this suit on November 6, 1985. She was told by three gynocologists in the early 1970s that her alleged medical problems may be related to depo-Provera. Additionally, the newspaper article about the plaintiff demonstrates, that at the very latest, in January of 1983 plaintiff knew that she was injured and *661 that in her opinion depo-Provera was the cause of her injury. Thus, since this action was filed over two years after the limitations period expired, defendant Upjohn argues it is entitled to summary jury as a matter of law.

In opposition plaintiff points out that she is “plagued with bleeding, prolonged hemorraging, infections, obesity, darkening of the skin, hair loss, Gray’s disease, fibroid tumors, iritis, fatty breast deposits, arthritis and depression ... In addition ... [she] was forced to have a hysterectomy in 1974” (doc. 29, p. 2). She contends that at the time she received injections of depoProvera none of her doctors administering the drugs informed her of possible short term or long term side effects nor did any of the gynecologists inform her “to a degree of medical certainty” that depo-Provera was a cause of her injuries described above. Plaintiff points out that depo-Provera had been used extensively as a contraceptive in over seventy countries and according to Upjohn’s statistics one and one-half million women received their first injections over ten years ago. However, the Food and Drug Administration (FDA) refused approval of a supplemental new drug application for depo-Provera for intramuscular injections as a contraceptive agent in humans. Plaintiff points out that in 1978 Upjohn challenged the FDA’s decision refusing approval and requested a public board composed of physicians to inquire into depo-Provera’s use as a contraceptive. The public board released its findings on October 17, 1984 denying approval:

The facts related to the long term consequences of the use of the drug are inadequate and insufficient to provide a basis for risk assessment. This is a serious deficiency in light of the specific questions that have been raised that the drug may have major adverse affects following its long term use or that may become evidenced only after a latent period. (Board of Inquiry Report at p. 172, Exh. C).

(doc. 29 at p. 3).

Plaintiff relies upon Harper v. Eli Lilly & Co., 575 F.Supp. 1359 (N.D.Ohio 1983). However, we think the facts in Harper are distinguishable. The Court recognized in Harper the difficulty in pinpointing the time when a latent injury claim accrues:

Where a party has allegedly been injured by a product whose toxicity has not produced any ascertainable injuries simultaneously with its contact with the plaintiff, the courts have allowed plaintiffs to initiate suit at the time when plaintiff’s later experiences a medically and legally cognizable injury.

Harper, 575 F.Supp. at 1361.

Harper involved diethylstibestrol (DES) a synthetic estrogen manufactured and marketed by the defendant. The plaintiffs during their teenage years suffered from vaginal infections, etc. Plaintiffs were treated for various conditions and over the next few years they continued to experience vaginal and urinary infections and irritations. Various creams and drugs were prescribed for her condition each time she sought medical attention.

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Bluebook (online)
686 F. Supp. 659, 1988 U.S. Dist. LEXIS 6145, 1988 WL 66070, Counsel Stack Legal Research, https://law.counselstack.com/opinion/longmire-v-upjohn-co-ohsd-1988.