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If you already supplement with fish oil, then you know how good it is for you: It contains two important essential fatty acids, EFA and DHA. But as healthy as fish oil is, you also know that the resulting "fish burps" are a thoroughly unpleasant experience. One thing I really like about T.H.E. Bar is that it provides an easy way to get your EFAs--without that fishy aftertaste. The omega-3 EFAs included in T.H.E. Bar are from ultra-refined fish that has no detectable levels of toxins, such as PCBs polychlorinated biphenyls ; , dioxins, and heavy metals--and, also important, no detectable taste. Patient's name, address, phone number, date of birth, height, and weight Allergies, insurance ID number, patient's diagnosis and appropriate ICD-9 CM code Factor prescribed include manufacturer, brand name, and HCPCS code ; Percentage level, inhibitor present, approximate number of units per dose, and doses per month. Incomplete information will result in a denial of services. See attached Hemophilia Patient Profile worksheet ; Additionally, the treating physician's name, provider number, date, and the provider's signature, must accompany the profile and prescription. NOTE: It is not appropriate for the profile to state "signature on file" ; . The prescription must be rewritten yearly. The patient is required to keep a flow sheet documenting the date, description of bleed, dose of factor injected, and any emergency situations requiring additional factors. This information should be available to the physician, supplier and carrier to assist in the updating of the yearly prescription and profile. All documentation must be available to Medicare upon request. Reversed and remanded with directions. Channel P. Townsley, of Hutton & Hutton, of Wichita, argued the cause, and Andrew W. Hutton, of the same firm, was with him on the briefs for appellants. Joe G. Hollingsworth, of Spriggs & Hollingsworth, of Washington, D.C., argued the cause, and Katharine R. Latimer, of the same firm, Wyatt M. Wright, of Foulston & Siefkin L.L.P., of Wichita, and Grant J. Esposito, of Mayer, Brown & Platt, of New York, New York, were with him on the brief for appellees. The opinion of the court was delivered by SIX, J.: This case reviews the district court's use of the Frye test, Frye v. U.S., 293 F. 1013 D.C. Cir. 1923 ; , to strike plaintiffs' expert causation opinions advanced to explain a mother's death 3 days after the delivery of her baby. Summary judgment was entered for defendant Sandoz Pharmaceuticals Corporation Sandoz ; . The plaintiffs, Gail Kuhn, the mother of Jennifer Kuhn Bishop, deceased, and as Special Administrator of her Estate; Jerry Bishop, the deceased's husband; and Ryan Thomas Kuhn Bishop, the deceased's minor son, appeal. The plaintiffs' underlying product liability negligence suit asserts wrongful death and survivor claims. The plaintiffs contend that the drug Parlodel, manufactured by Sandoz, caused or contributed to Jennifer's death. The district court reasoned that all of plaintiffs' experts' causation opinions and all studies, literature, and other evidence on which plaintiffs' experts relied was unreliable as a matter of law. Our jurisdiction is under K.S.A. 20-3018 c ; , a transfer on our order from the Court of Appeals. We review whether the district court committed error by: 1 ; granting summary judgment in favor of Sandoz based on the failure of medical causation proof and 2 ; reasoning that the opinions on causation expressed by plaintiffs' experts failed the Frye test. Genuine issues of material fact remain. We reverse and remand. The Frye test is not applicable to the expert causation opinions at issue here. FACTS Jennifer Bishop gave birth to a baby boy at 7: 47 a.m. on July 25, 1993, in the Hays, Kansas, hospital. Because Jennifer had decided not to breast-feed her baby, she received a 2.5 mg. tablet of Parodel at 5: 30 p.m. during dinner on that day to prevent postpartum lactation the production of breast milk. ; She vomited at 6: 15 p.m., was overcome by nausea at 6: 30 p.m., experienced chills and elevated blood pressure at 6: 40 p.m., and vomited again at 7 p.m. By 7: 30 p.m., Jennifer's temperature increased to 102.3 degrees Fahrenheit. She vomited again at 7: 40 p.m. and continued to complain of a headache and chilling. At 9 p.m., she was drowsy and could not open her left hand on request. At 9: 30 p.m., she screamed and became stiff and less responsive. Jennifer remained rigid over the next 30 minutes, relaxing only when she was given Benadryl at 10: 13 p.m. At 10: 45 p.m., she was transferred to the intensive care unit, suffered a respiratory arrest, and lapsed into a coma. She was pronounced dead at 3: 30 p.m. on July 28, 1993. The autopsy reported that the probable cause of the death was "related to postpartum eclampsia" or "possible bacteremia." Definitions are appropriate here to assist the reader: "postpartum" "[a]fter childbirth" ; , "eclampsia" the "[o]ccurrence of one or more convulsions, not attributable to other cerebral conditions such as epilepsy or cerebral hemorrhage, in a patient with preeclampsia" ; , and "bacteremia" a condition characterized by "viable bacteria in the circulating blood" ; . Stedman's Medical Dictionary 26th ed. 1995 ; , pp. 1413, 540, 181. The autopsy description of Jennifer's central nervous system stated that sections of the cerebrum and cerebellum showed "hyperemia and some diffuse edema and possible petechial hemorrhage" and that sections of the brain stem "demonstrate[d] softening and mild edema with hyperemia." The following definitions apply: "hyperemia" "[t]he presence of an increased amount of blood in a part or organ" ; , "edema" "[a]n accumulation of an excessive amount of watery fluid in cells, tissues, or serious cavities" ; , and "petechial" a condition characterized by "[m]inute hemorrhagic spots, of pinpoint to pinhead size, in the skin" ; . Stedman's at 824, 544, 1337. Jennifer's discharge summary listed the final diagnosis regarding her death as "Bacteria with Strep Group D, " a condition that brought about "cerebral edema and probable herniation of the brain stem secondary to postpartum toxemia." "Toxemia" refers to the "[c]linical manifestations observed during certain infectious diseases, assumed to be caused by toxins and other noxious substances elaborated by the infectious agent lay term referring to the hypertensive disorders of pregnancy." Stedman's at 1826. ; The plaintiffs sued Sandoz , the manufacturer of Parlodel, on July 16, 1996. DISCUSSION The FDA Report.

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