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Introduction to the instructions for dextromethorphan hydrobromide oral solution

Version: Sample instructions for non-prescription drugs published by the State Food and Drug Administration in 2007

Description: The instructions for dextromethorphan hydrobromide oral solution were published by the State Food and Drug Administration in January 2007. On March 31, the "Notice on the Release of Sample Instructions for Over-the-Counter Drugs" No. 54 [2007] of the State Food and Drug Administration was released.

Drug Name

Generic Name: Dextromethorphan Hydrobromide Oral Liquid

Trade Name:

English Name:

Chinese Pinyin:

Ingredients

Properties

Category of action

This product is an over-the-counter antitussive drug.

Indications

For dry cough, including cough caused by upper respiratory tract infections (such as colds and pharyngitis), bronchitis, etc.

Specifications

0.20%

Usage and dosage

Orally administered. Children and adults over 12 years old: 10 to 15 ml once, 3 to 4 times a day.

The dosage for children under 12 years old is shown in the table below:

Age (years) Standard weight (kg) Single dosage (ml) Frequency

13 1015 1.5~2 3 to 4 times a day

46 Reactions

Dizziness, headache, drowsiness, irritability, belching, lack of appetite, constipation, nausea, skin allergies, etc. may be seen, but the efficacy will not be affected. The above reactions may disappear on their own after stopping the drug. Overdose can cause confusion, bronchospasm, and respiratory depression.

Taboos

1. It is prohibited for women within 3 months of pregnancy, those with a history of mental illness and lactating women.

2. It is contraindicated in patients who have stopped taking monoamine oxidase inhibitors for less than two weeks.

Precautions

1. Please consult a physician when using this product for children under 1 years old.

2. If the symptoms are not relieved after taking the medicine for 7 days, please consult a doctor or pharmacist.

3. Patients with asthma, excessive phlegm, and patients with liver and kidney dysfunction should use with caution.

4. Pregnant women should use with caution.

5. While taking medication, you are not allowed to drive machines, vehicles, boats, engage in high-altitude operations, mechanical operations, or operate precision instruments.

6. People who are allergic to this product should not use it, and people with allergies should use it with caution.

7. It is prohibited to use this product when its properties change.

8. Please keep this product out of the reach of children.

9. Children must use it under adult supervision.

10. If you are using other drugs, please consult your physician or pharmacist before using this product.

Drug interactions

1. It should not be used together with monoamine oxidase inhibitors and antidepressants.

2. This product should not be used together with ethanol and other central nervous system depressant drugs, as it can enhance the inhibitory effect on the central nervous system.

3. Drug interactions may occur if used together with other drugs. Please consult your physician or pharmacist for details.

Storage

Packaging

Validity period

Implementation standards

Approval number

Instruction Revision Date

Manufacturer

Company name: Production address: Postal code: Telephone number: Fax number: Website:

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