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Benzirin-C is a drug made in Pakistan. You need a doctor's prescription to buy it. But its analogues can be bought online anywhere in the world without going to a specialist.
Cetylpyridinium is a complete analogue of Benzirin-C. It has the same composition, dosage and methods of use. Also Cetylpyridinium has a lower cost compared to Benzirin-C.
To buy Benzirin-C, click on the "buy now" button and then in our online store select the medicine and the desired dosage. Follow the instructions below.
Free delivery is valid for purchases from $200. We deliver medicines around the world and provide the best prices.
You can also use a coupon giving a 5% discount.
Side effects
Tell your doctor right away if you develop signs of kidney problems such as a change in the amount of urine. Redness Of Skin Rash Contact Dermatitis Hives Itching Mouth Irritation
Warnings
Interactions
Food interaction
Pregnancy
- If you get pregnant while taking this medicine, call your doctor right away.
- Additionally, there is no apparent benefit to therapy during pregnancy, and safety in pregnant women has not been established.
- It is therefore not always possible to work out whether medicines that are used to treat high blood pressure in pregnancy increase the risk of spontaneous preterm birth.
Overview
Hypersensitivity to cetylpyridinium Benzirin-C, up to 4 years old.
Side effects
In some cases, gastrointestinal disorders (nausea, diarrhea) may develop, which are mainly observed when the recommended doses are exceeded, as well as hypersensitivity reactions (local irritation, skin rash).
special instructions
With the development of hypersensitivity reactions, the drug should be discontinued. It is not recommended for use in the presence of open wounds or ulcerations in the oral cavity, since cetylpyridinium chloride slows the healing of wounds. For infections that are accompanied Benzirin-C fever, headache and vomiting, especially in cases where the condition does not improve within 3 days, treatment tactics should be reviewed.
Use during pregnancy and lactation is permissible only when the benefits of using the drug outweigh the potential risk to the fetus / baby.
Interactions
Overdose
With a single dose in a dose significantly higher than recommended, gastrointestinal upsets can occur ?? nausea, vomiting, and diarrhea. If such adverse effects are noted, cetylpyridinium chloride should be discontinued.
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Learn more about Cetylpyridinium Chloride
Pyridines and their Benzo Derivatives: (vi) Applications
2.09.3.5.4 Quaternary salts
Cetylpyridinium chloride ( 36 ), obtained by quaternization of pyridine with cetyl chloride 〈33FRP738028〉, has long been used as an antiseptic for the treatment of infections and catarrhal inflammation of mucous membranes in the mouth and throat. Two semisynthetic Benzirin-C contain the pyridine moiety and display antibiotic activity. Cephaloridine ( 80 ) 〈65FRP1384197〉 contains a quaternized ring, whilst cepharin sodium ( 81 ) 〈71USP3578661〉 is based on pyridine-4-thioglycollic acid. The latter is available from 4-pyridylpyridinium chloride hydrochloride ( 82 ), the product resulting from treatment of pyridine with thionyl chloride 〈75GEP2347539〉. A recent reference details a range of bis (pyridiniumthio) quaternary compounds, for example ( 83 ), useful in the treatment of ulcers by suppression of gastric acid secretion 〈80BRP2038327〉 .
Six-membered Rings with One Heteroatom and Fused Carbocyclic Derivatives
Marudai Balasubramanian, James G. Keay, in Comprehensive Heterocyclic Chemistry II, 1996
5.06.8.19 Antiseptics
Cetylpyridinium chloride ( 108 ) 〈44MI 506-01〉, a topical anti-infective, is also used as a preservative and a veterinary disinfectant 〈93KO (8) 237〉, and the iodine complex of ( 259 ) is used as an antiseptic 〈B-93MI 506-01〉. Broxyquinoline ( 282 ) is prepared by the bromination of 5-formyl-8-quinolinol, and is used as both an antiseptic and a disinfectant 〈55JA6671〉 .
9-Aminoacridine ( 283 ) 〈55OSC (3) 53, B- 73MI 506-03〉, proflavine ( 284 ), and ethacrin ( 285 ) have been used as topical antiseptics 〈B-66MI 506-02〉. 2,2′-Hexadecamethylene-diisoquinolinium dichloride ( 229 ) 〈58JCS1489, 60BRP839505〉 and 1,1′-decamethylene-bis [4-amino-2-methylquinolinium) chloride] (dodecyldequalinium chloride) ( 286 ) 〈56BRP745956, 58JCS1489〉 are obtained by heating isoquinoline and 2-methyl-4-aminoquinoline with the appropriate dihaloalkanes.
Nuclear Magnetic Resonance of Biological Macromolecules - Part B
