Papaverine Hydrochloride for Injection
Function and Efficacy
Pharmacological action: Papaverine hydrochloride has a relaxant effect on visceral and vascular smooth muscles, directly inhibiting abnormal tension and spasm of smooth muscles, especially the spasmodic contraction of smooth muscles.
Ingredients
1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline hydrochloride
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| Papaverine hydrochlorideIngredients |
It has a relaxant effect on visceral and vascular smooth muscles, directly inhibiting abnormal tension and spasm of smooth muscles, especially the spasmodic contraction of smooth muscles. More |
61-25-6 | 16 |
Appearance
This product is white loose mass or powder.
Indication
This product is a vasodilator. It is used to treat ischemia caused by spasm of the brain, heart and peripheral blood vessels, and spasm of the kidneys, gallbladder or gastrointestinal tract and other internal organs.
Usage and Dosage
Each vial of this product must be completely dissolved with an appropriate amount of injection water before use. The usual dosage for adults is slow intramuscular injection, 30 mg at a time, 90-120 mg per day. Intravenous injection, 30-120 mg at a time, once every 3 hours, should be injected slowly, not less than 1-2 minutes, to avoid arrhythmia and fatal suffocation. When used for cardiac arrest, the two doses should be separated by 10 minutes. Slow intravenous drip, diluted with 0.9% sodium chloride injection and dripped, 30 mg at a time (calculated as papaverine hydrochloride), 90-120 mg per day, divided into 3-4 doses.
Adverse Reactions
1. Jaundice may occur after medication, manifested as obvious yellowing of the eyes and skin, indicating liver damage. 2. Nausea, vomiting, loss of appetite, constipation, headache, drowsiness and allergic reactions may occur. 3. Redness, swelling or pain of the skin at the injection site may occur. Rapid administration may cause deeper breathing, flushing, accelerated heartbeat, hypotension and dizziness. 4. Overdose may cause blurred vision, diplopia, drowsiness or (and) weakness. 5. Increased blood eosinophils, alanine aminotransferase, alkaline phosphatase, aspartate aminotransferase and bilirubin may occur.
Storage
Keep in a light-proof and sealed container. The validity period is tentatively 18 months.
Packaging Specification
30mg
Manufacturer
Harbin Medical University Pharmaceutical Co., Ltd.
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Founded in:
1998-04-08 -
Address:
Bohai Road, Central Area, Haping Road, Harbin Development Zone -
Tax NO.:
91230199702953105L -
Registered Funds:
56.9258 million yuan -
Website:
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Email: