Prothiodine Injection
Function and Efficacy
This product is an organic iodide, an auxiliary therapeutic drug that promotes the absorption of pathological turbidity. It is absorbed slowly after injection. Most of it exists in adipose tissue and nerve tissue, and gradually decomposes into free iodine in the body and distributes throughout the body. It can promote the absorption of inflammatory exudates and other pathological deposits in tissues and the dissipation of chronic inflammation.
Ingredients
Main ingredient: Proiodine; chemical name: (2-hydroxy-1,3-propylene) bis(trimethylammonium) diiodide.
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| 2-HYDROXY-N,N,N,N',N',N'-HEXAMETHYL-1,3-PROPANE DIAMINIUM DI IODIDEIngredients |
This product is an organic iodide, an auxiliary therapeutic drug that promotes the absorption of pathological turbidity. It is absorbed slowly after injection. Most of it exists in adipose tissue and nerve tissue, and gradually decomposes into free iodine in the body and distributes throughout the body. It can promote the absorption of inflammatory exudates and other pathological deposits in tissues and the dissipation of chronic inflammation. More |
123-47-7 | 3 |
Appearance
This product is a colorless clear liquid.
Indication
It is used for late-stage granulomatous or non-granulomatous iridocyclitis, retinal choroiditis, fundus hemorrhage, vitreous opacities, semi-old corneal leukoplakia, and leukoma. It can also be used as an adjuvant treatment for optic neuritis.
Usage and Dosage
1. Subconjunctival injection of 0.1-0.2g, once every 2-3 days, 5-7 times as a course of treatment. 2. Intramuscular injection of 0.4g, once every day or every other day, 10 times as a course of treatment, 7-14 days between each course of treatment, generally 2-3 courses of treatment.
Adverse Reactions
Long-term use may occasionally cause mild iodine poisoning symptoms, such as nausea, itching, skin rash, etc. When symptoms occur, stop using the product or use it less frequently.
Precautions
1. Patients who are allergic to iodine are contraindicated. 2. Patients with severe liver and kidney dysfunction, active pulmonary tuberculosis, and occult bleeding from peptic ulcers are contraindicated. 3. Patients with gonadal enlargement and a family history of hyperthyroidism should use with caution.
Special Population Medication
Precautions for children: This experiment has not been conducted and there is no reliable reference. Precautions for pregnancy and lactation: This experiment has not been conducted and there is no reliable reference. Precautions for the elderly: This experiment has not been conducted and there is no reliable reference.
Drug Interactions
This experiment has not been conducted and there are no reliable references.
Storage
Keep away from light and store in a sealed container.
Packaging Specification
2ml:0.4g
Validity Period
36 months
Manufacturer
Shanghai Fuda Pharmaceutical Co., Ltd.
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Founded in:
1994-06-15 -
Address:
No. 1000, Yunhe North Road, Nanqiao Town, Fengxian District, Shanghai -
Tax NO.:
91310120134003418G -
Registered Funds:
16 million yuan -
Email: