Maryland Code § HG-13-3108

Section HG-13-3108
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(a) An individual who administers an opioid overdose reversal drug
approved by the federal Food and Drug Administration to an individual who is or in
good faith is believed to be experiencing an opioid overdose shall have immunity from
liability under §§ 5-603 and 5-629 of the Courts Article.
(b) A cause of action may not arise against any licensed health care provider
with prescribing authority or pharmacist for any act or omission when the health care
provider with prescribing authority or pharmacist in good faith prescribes or
dispenses an opioid overdose reversal drug approved by the federal Food and Drug
Administration and the necessary paraphernalia for the administration of the opioid
overdose reversal drug approved by the federal Food and Drug Administration to an
individual under § 13-3106 of this subtitle.
(c) A cause of action may not arise against any business or business owner
for any act or omission when the business or business owner in good faith makes
opioid overdose reversal drugs approved by the federal Food and Drug Administration
available to the employees or patrons of the business along with the necessary
paraphernalia for administration of the opioid overdose reversal drugs approved by
the federal Food and Drug Administration to an individual under § 13-3104 or § 13-
3106 of this subtitle.
(d) This subtitle may not be construed to create a duty on any individual to:
(1) Obtain education and training from an authorized private or
public entity under this subtitle, and an individual may not be held civilly liable for
failing to obtain education and training from an authorized private or public entity
under this subtitle; or
(2) Administer opioid overdose reversal drugs approved by the
federal Food and Drug Administration to an individual who is experiencing or
believed by the individual to be experiencing an opioid overdose.

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