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Apomorphine hydrochloride sublingual tablets

Function and Efficacy

Apomorphine hydrochloride binds to dopamine receptors in the hypothalamus, and transmits electrical impulses from the hypothalamus to the spinal cord through the paraventricular nucleus of the hypothalamus, which controls sexual desire, to promote blood flow to the penis. At the same time, it also affects the activation of nitric oxide, causing it to be absorbed and then transported to the brain, causing a series of chain reactions in the human body, and finally increasing blood flow and causing penile erection.

Ingredients

Apomorphine hydrochloride, its chemical name: (R)-6-methyl-5,6,6α,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diphenol hydrochloride hemihydrate. Molecular weight: C17H17NO2

Name Description Content CAS NO. Manufacturer
APOMORPHINE HYDROCHLORIDEIngredients

It binds to dopamine receptors in the hypothalamus, transmits electrical impulses from the hypothalamus to the spinal cord through the paraventricular nucleus of the hypothalamus, which controls sexual desire, and promotes blood flow to the penis. At the same time, it affects the activation of nitric oxide, causing it to be absorbed and then transported to the brain, causing a series of chain reactions in the human body, and finally increasing blood flow and causing penile erection.

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314-19-2 8

Appearance

This product is white or off-white flakes, which gradually turn green in air or sunlight.

Indication

This product is suitable for the treatment of male erectile dysfunction.

Usage and Dosage

Dissolve the drug sublingually 20 minutes before sexual intercourse, usually about 10 minutes. If it is not completely dissolved after 20 minutes, swallow it. Drink a small amount of water before taking the drug to moisten the mouth and make the drug easier to dissolve. Initial dose: The recommended initial dose for all patients is 2 mg. Adjust the dose: If the therapeutic effect is not achieved, the dose can be adjusted to 3 mg at a time. Elderly patients do not need to adjust.

Adverse Reactions

This product has mild transient adverse reactions. Possible adverse reactions include nausea, headache, dizziness, drowsiness, pharyngitis, aggravated cough, arthritis, facial flushing, abnormal taste, sweating, etc. Fainting is occasionally seen.

Precautions

1. Those who are allergic to any component of this product. 2. Those with severe variant angina, new myocardial infarction, severe heart failure, hypotension, or other physical conditions that are not suitable for sexual activity. 3. Those whose sexual partners are pregnant or breastfeeding women.

Special Population Medication

Precautions for children: This product is not suitable for children and adolescents under 18 years old. Precautions for pregnancy and lactation: This product is not suitable for pregnant and lactating women. Precautions for the elderly: Elderly patients do not need to adjust.

Drug Interactions

1. This product may interact with nitrate drugs. 2. This product should be used with caution with drugs for the treatment of hypertension. 3. This product should not be used with other central dopamine receptor agonists or antagonists. 4. Drinking alcohol after taking the drug can increase the incidence and degree of hypotension and reduce the effectiveness of this product. 5. This product has no interaction with ondansetron, prochlorperazine maleate, domperidone and other drugs. 6. There is no systematic study on the interaction between this product and antidepressants, anticonvulsants or other central nervous system drugs, but no interaction has been found in clinical practice.

Storage

Keep away from light and store in sealed container.

Packaging Specification

3mg*4s

Validity Period

24 months

Manufacturer

Hubei KEYI Pharmaceutical Industry Co., Ltd.

  • Founded in:

    1997-05-23
  • Address:

    No. 8, Huanglongshan South Road, East Lake New Technology Development Zone, Wuhan
  • Tax NO.:

    91420000726103295U
  • Registered Funds:

    34.750206 million yuan
  • Email:

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