Page 5 - Ministerial Resolution No. (14) of 2021
P. 5

understanding  and  dialogue  when  dealing  with  certain  categories  of  patients
                       (children, psychiatric patients and the elderly).

                   Patients shall be informed:

                         While being at the clinic or during a special session.
                         While being hospitalized in the health facility.
                         Upon leaving the health facility, to urge him/her to continue treatment, take
                          preventive measures and avoid complications that may cause health setback to

                          his/her condition.


                       The patient has the right to be informed of the following:

                         Various examinations, proposed treatments and necessary preventive services.
                         The benefits and estimated cost of the proposed course of treatment in advance.
                         The urgency of implementation of the proposed health services to be provided.
                         The expected results from the proposed health service.
                         Possible alternatives to the proposed health service.
                         The expected results in case of refusal of the health services.
                         Reasons for his/her transfer from a health facility to another.
                   The  physician  may  be  exempted  from  providing  information  to  the  patient  in
                   emergencies, or in case that the patient refuses to know such information, or when

                   his/her interest so requires.

                     The patient's informed consent must be obtained to receive the health service in
                       advance, subject to the exceptions specified by law.
                     The  right  to  consent  to  the  health  service belongs  to  the patient  or  his/her
                       legal representative if the patient is incapacitated or restricted.
                     Before carrying out a medical experiment on any person,  his/her written consent
                       must  be  obtained  after  being  informed  of  the  experiment  purpose,  method  and
                       duration, in addition to the undesirable effects it may have, and, in all cases, the
                       conditions  and measures specified in the applicable legislation in the country must
                       be adhered to.
                     Personal health information and data are owned by the patient and protected within
                       the  scope  of  the  preservation  of  the  medical  confidentiality  that  may  only  be
                       disclosed to third parties under the patient's permission or in cases required by law.
                     The physician must provide the patient of information and data related to his/her
                       health  and  not  maintain  medical  confidentiality,  except  in  accordance  with  the
                       conditions and in the cases stipulated in the applicable legislation.
                     A family, a relative or a person who enjoys the patient's trust and appointed for this
                       purpose may be notified, when a serious development of his/her health condition is
                       expected, unless the patient has prevented the same in advance.







                     *In case of any misinterpretation, the Arabic version of this legislation prevails.
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