cases) than by intramuscular injection (18 cases), and
the rationality of this needs to be discussed.
3.6 Repeated Medication
Among the Chinese proprietary medicines for the
treatment of wind-heat colds, there was a high rate of
duplication in Scutellaria baicalensis Georgi,
Forsythia suspensa, Platycodon grandiflorus, and
Lonicera japonica Thunb. flowers, and the combined
medication may pose a risk of overdose for patients.
Some medications contain a toxic component, poppy
husk. Modern pharmacological and chemical studies
have shown that the main pharmacological
components of poppy husk herbs are alkaloids, such
as morphine, narcotine, codeine, papaverine, and
protopine, which have significant analgesic and anti-
cough effects (Nanjing University of Chinese
Medicine, 2006; Chinese Pharmacopoeia
Commission, 2010). Codeine has pharmacological
effects similar to morphine and is an addictive and
respiratory depressant. It is one of the ten low
addictive narcotic medications considered by the
United Nations. Thus, it needs to be considered in the
actual administration whether the patient is taking an
excessive amount of codeine when using Lung-
Clearing and Cough-Stopping Mixture, which
contains a certain amount of poppy husk, in
combination with Compound Codeine Platycodon
Tablets.
4 CONCLUSION
Chinese proprietary medicine has been widely used in
clinical due to its remarkable curative effect, small
toxic side effects and convenient administration. In
the outpatient prescriptions of acute URTI in our
hospital from January to June 2021, 85% of the
prescriptions used Chinese proprietary medicine, and
the qualified rate of prescriptions reached 97.73%.
The results showed that the use of Chinese
proprietary medicines in the prescriptions for treating
acute URTI was basically reasonable. Whereas the
problems of unreasonable prescriptions should be
paid attention to, and the training of TCM theory for
physicians should be strengthened. The prescription
analysis also found that the proportion of Chinese
proprietary medicines in children's use was large.
Therefore, attention should be paid to the use of
children's drugs. It is suggested that drug R&D
enterprises should develop doses suitable for children
and improve clinical trials.
ACKNOWLEDGMENTS
This work was supported by the College Students'
Innovative Entrepreneurial Training Plan Program of
Jiangxi Science and Technology Normal University
(No. 202115041113, No. 20201404119) and the
Innovation Special Fund Project of Graduate (No.
YC2021-X21).
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