Allberry v. Parkmor Drug, Inc.

834 N.E.2d 199, 2005 Ind. App. LEXIS 1744, 2005 WL 2243156
CourtIndiana Court of Appeals
DecidedSeptember 16, 2005
Docket20A03-0503-CV-125
StatusPublished

This text of 834 N.E.2d 199 (Allberry v. Parkmor Drug, Inc.) is published on Counsel Stack Legal Research, covering Indiana Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Allberry v. Parkmor Drug, Inc., 834 N.E.2d 199, 2005 Ind. App. LEXIS 1744, 2005 WL 2243156 (Ind. Ct. App. 2005).

Opinion

OPINION

BAILEY, Judge.

Case Summary

Appellant-Plaintiff Albert Allberry ("Allberry") appeals the trial court's grant of summary judgment in favor of Appel-lee-Defendant, Parkmor Drug, Inc. d/b/a Park Pharmacy ("Parkmor"). We affirm. 1

Issue

Allberry raises two issues on appeal, which we consolidate and restate as whether Parkmor owed a duty to Allberry to either warn him of the potential side effects associated with a particular prescription drug or, in the alternative, provide Allberry with the manufacturer's product information.

Facts and Procedural History

On or before June 1, 2002, Allberry purchased the prescription drug Caverject-which is generally used to treat impotence-from Parkmor. At the time, Park-mor did not give Allberry "any product information" from the drug's manufacturer or any "drug information, leaflets, [or] pamphlets." Appellant's App. at 19. In addition, Parkmor did not warn Allberry about the adverse side effects associated with the use of Caverject. In particular, Parkmor did not advise Allberry to seek medical attention if, after using the drug, he had an erection for more than four hours.

On June 1, 2002, after injecting Caver-ject into his penis, Allberry experienced a "severely painful erection which lasted for almost 72 hours." Id. On June 2, 2002, Allberry had to undergo surgery to reduce the erection. After his surgery and upon inquiry to Parkmor, Allberry's wife received the "patient information leaflet," which contains the following, pertinent information: "The erection should last about one hour. If an erection lasts more than 4 hours, seek immediate medical attention. If you notice other effects not listed above, contact your doctor or pharmacist." Id. at 28. As a result of the incident, Allberry developed "priapism and later became impotent." Id. at 20.

On July 28, 2004, Allberry filed an amended complaint against Parkmor, alleging, in part, that the pharmacy had failed to provide him with any warnings regarding the adverse side effects of the prescription drug Caverject. On August 19, 2003, Parkmor filed its second motion to dismiss, which the trial court treated as a motion for summary judgment. On February 9, 2004, the trial court granted summary judgment to Parkmor with respect to *201 Allberry's failure to warn claim. Subsequently, Allberry agreed to dismiss his remaining claim against Parkmor-ie., that Parkmor had improperly filled his prescription-and the trial court's February 9th order became a final appealable order. Allberry now appeals.

Discussion and Decision

I. Summary Judgment Standard of Review 2

On review of a trial court's decision to grant or deny summary judgment, we apply the same standard as the trial court: we must decide whether there is a genuine issue of material fact that precludes summary judgment and whether the moving party is entitled to judgment as a matter of law. Carie v. PSI Energy, Inc., 715 N.E.2d 853, 855 (Ind.1999). Once the moving party has sustained its initial burden of proving the absence of a genuine issue of material fact and the appropriateness of judgment as a matter of law, the party opposing summary judgment must respond by designating specific facts establishing a genuine issue for trial. Stephenson v. Ledbetter, 596 N.E.2d 1369, 1371 (Ind.1992). We may consider only those portions of the pleadings, depositions, and any other matters specifically designated to the trial court by the parties for purposes of the motion for summary judgment. Ind. Trial Rule 56(C), (H). Any doubt as to the existence of an issue of material fact, or an inference to be drawn from the facts, must be resolved in favor of the nonmoving party. Cowe v. Forum Group, Inc., 575 N.E.2d 630, 633 (Ind.1991). Although the nonmovant has the burden of demonstrating that the grant of summary judgment was erroneous, we carefully assess the trial court's decision to ensure that the nonmovant was not improperly denied his or her day in court. Colonial Penn Ins. Co. v. Guzorek, 690 N.E.2d 664, 667 (Ind.1997).

IIL Analysis

On appeal, Allberry argues that the trial court erroneously granted summary judgment to Parkmor because, as his pharmacist, Parkmor owed a duty of care to warn him of the adverse side effects of Caver-ject. In the alternative, Allberry contends that the grant of summary judgment was erroneous because, at the very least, Park-mor had a duty to provide him with the manufacturer's product information on the drug at issue. We disagree and, in so doing, reaffirm our holding in Ingram v. Hook's Drugs, Inc., 476 N.E.2d 881, 885 (Ind.Ct.App.1985), reh'g denied, trans. denied.

Here, the undisputed evidence demonstrates that the relationship between Park-mor and Allberry was that of a pharmacy and its customer. The designated evidence also reveals that the drug in question, i.e., Caverject, was prescribed to Allberry by his physician 3 and, further, that the prescription itself contained only the following language: "Caverject 40 mgl,] use as directed[,] 1 bottle." Appellant's App. at 22. Our task, then, is to determine whether, as a matter of law, Parkmor had a duty to warn Allberry of the side effects associated with Caverject, which was prescribed by his physician.

*202 In Ingram, 476 N.E.2d at 885, another panel of this Court determined that a pharmacist has no duty to warn a consumer of the possible side effects associated with a prescription drug prescribed by a physician. The Ingram court concluded that physicians, not pharmacists, are in the better position to weigh the potential risks and rewards of particular medications for specific patients and, thus, declined to impose a duty upon pharmacists to warn customers about the potential side effects of medication unless such warnings were included in the prescription received from the physician. Id. at 886-87; see also Hooks SuperX, Inc. v. McLaughlin, 642 N.E.2d 514, 518 (Ind.1994) (affirming that the responsibility of warning patients about drug side effects lies with physicians but imposing a duty where the pharmacist had personal knowledge that the customer was taking medication more quickly than prescribed). Indeed, the Ingram court reasoned:

[TJhe duty to warn of hazards associated with prescription drugs is part and parcel of the physician-patient relationship because it is best appreciated in this context. The decision of weighing the benefits of a medication against potential dangers that are associated with it requires an individualized medical judgment. This individualized treatment is available in the context of a physician-patient relationship which has the benefits of medical history and extensive medical examinations.

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Stephenson v. Ledbetter
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834 N.E.2d 199, 2005 Ind. App. LEXIS 1744, 2005 WL 2243156, Counsel Stack Legal Research, https://law.counselstack.com/opinion/allberry-v-parkmor-drug-inc-indctapp-2005.