Product liability claims involving pharmaceutical drugs. Limitation on sale of pseudoephedrine, FDA. Web sourcesįorms of ID accepted at pharmacies to pick up a controlled substance, NABP. Court ruled that damages in excess of $50 million were not excessive. 272 (2015)įailure to warn case involving children's Motrin. "Applying general principles of tort law and as a matter of public policy, this court concluded that a brand-name drug manufacturer that controls the contents of the warning label on a generic drug, as required by Federal law, owes a duty to consumers of that generic drug not to act in reckless disregard of an unreasonable risk of death or grave bodily injury." 141 (2018)Ĭase discusses the liability of a manufacturer of a brand-name drug for injuries caused by an inadequate warning label on a generic version of the drug. 214 (2003): Court held that the CVS pharmacist had a duty to warn the plaintiff that taking Ciproflaxin and Theophylline together could potentially result in adverse effects. In addition, a pharmacy may have a duty to warn if it has specific knowledge of increased danger to a particular customer, such as filling 2 prescriptions which adversely interact with each other. A pharmacy which voluntarily assumes the duty to warn, however, such as by providing a list of a drug's side effects, must exercise reasonable care. Only a physician, not a pharmacy or a drug manufacturer, has a duty to warn a customer about a drug's side effects. As a result, a pharmacy has the duty only to fill the prescription correctly. 316 (2002)Ĭourt described the "learned intermediary doctrine" wherein a physician acts as a "learned intermediary" between the drug manufacturer or distributor and the consuming patient. Traveling out of the country with prescription medicineĬottam v. Information on prescription drug addiction. States allowing a pharmacist to administer vaccines Orange book: approved drug products with therapeutic equivalence evaluations, U.S. Massachusetts policy on drug interchangeability This fact sheet highlights recent amendments to the MA Controlled Substances Act and also includes other sections of the statute, written in plain English. The MCSR provides accountability for the manufacture, distribution, dispensing, possession, prescribing, and administering of controlled substances which, in Massachusetts, includes all prescription drugs. The Drug Control Program issues the Massachusetts Controlled Substances Registration (MCSR) to health care facilities, manufacturers, distributors, community-based programs, and other entities as well as to individual health care providers and researchers. Massachusetts Controlled Substances Registration (MCSR) Massachusetts Board of Registration in Medicine's prescribing practices policy and guidelines (2015)Ī comprehensive overview of the physician's responsibilities related to physicians' prescribing practices including prescribing to family and friends, and internet prescriptions. List of drugs needing a prescription and a list of exemptions Procedure for requesting the removal of a person’s license to have or carry a gun due to prescription drug misuse. Portal to information on safety, shortages, and recalls. Food and Drug Administration.ĭrug safety and availability, U.S. Insurance providers cannot: make a patient try medications that are known to be either ineffective or cause adverse reactions make a patient repeat step therapy with the same medication or one in the same pharmacological class and providers must approve or deny exemption requests and appeals by 3 business days (or in 24 hours in an emergency).ĭrug approvals and databases, U.S. 2022, c.254 An act relative to step therapy and patient safety MGL c.118E, § 51A Clinical review criteria used to establish step therapy protocol requests for exceptions to protocol (Effective October 1, 2023) MGL c.118E, § 13L Hospitals can buy prescription drugs at discounted prices MGL c.175H, § 3 Using prescription drug coupons
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