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Medical
Malpractice News
Medication Error Death
Legal Issues Regarding Medications Errors Approximately 30% of all malpractice claims involve drug-related injuries. An average payment of $99,721 was made for 2,195 out of the 6,646 claims reported to the Physician Insurers Association of America during the period 1985 through 1992.4 Anyone who manufactures, sells, distributes, prescribes, dispenses, or administers drugs, as well as the health care facility that employs them or places the medication in their formulary can be sued for subsequent patient injuries.
Theory of Liability Health care providers sued for medication errors generally incur liability under the theory of negligence. Negligence is a tort that relates to an injury caused by conduct that deviates from a “standard of care.” Medical malpractice is a type of negligence that denotes an injury to a patient caused by a health care provider’s conduct that deviates from a professional standard of care. In a malpractice claim of a medication error, a jury assesses a health care provider’s behavior to determine whether it adhered to the professional standards of practice required by both his profession and the law.
Example Case: The patient immediately had a reaction and died 16 days later. The patient’s family sued the physician, the hospital, and the nursing, clerical and pharmacy staff. Prior to trial the resident settled the claim against him for $230,000. At trial it was learned that the defendants relied on a computer generated Medication Administration Record (MAR) which listed “no allergies” for the patient. The defendants failed to thoroughly review the patient’s medical records for allergies or check the MARs for any inconsistencies. The court concluded that the defendant health care providers had failed their responsibilities to verify the appropriateness of the patient’s prescriptions and to bring potential problems to the attention of the prescriber. The plaintiffs were awarded $350,000 in damages.
FDA receives medication error reports on marketed human drugs
You can see FDA drug reports at fda.com . Problems from drugs can include: professional practice, health care products, procedures, and systems, including prescribing; order communication; product labeling, packaging, and nomenclature; compounding; dispensing; distribution; administration; education; monitoring; and use.
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Definition:
A statute of a US state or jurisdiction that outlines the scope of practice for physicians and the responsibility of the medical board to regulate that practice. The primary responsibility and obligation of a state medical board is to protect the public through proper licensing and regulation of physicians and, in some jurisdictions, other health care professionals.
Tort Liability
Definition:
The defendant must owe a legal duty to the victim, the defendant breached that duty, the breach was the cause of an injury to the victim, there must be an injury. In most cases, there must be a physical or financial injury to the victim, but sometimes emotional distress, embarrassment, or dignitary harms are adequate for recovery.
Collateral source rule
Definition:
Under this rule, compensation awarded to an injured party shall not be reduced by the amount of compensation available to him from his insurance company or other independent sources.
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