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The risks of aspirin late in pregnancy are probably not relevant for a topical exposure to salicylic acid, even late in the pregnancy, because of its low systemic levels. Topical salicylic acid is common in many over-the-counter dermatological agents and the lack of adverse reports suggests a low risk. [9]
Trolamine salicylate (Aspercreme, Aspergel) is an organic compound with the chemical formula [HN(CH 2 CH 2 OH) 3] + C 6 H 4 (OH)(COO −).It is a salt of triethanolamine and salicylic acid, i.e. the compound consists of protonated triethanolamine and the conjugate base of salicylic acid, salicate.
Severe side effects include liver problems and allergic reactions. [1] Liver injury is, however, unusual. [6] Oral use during pregnancy is not typically recommended. [1] The cream and ointment may result in itchiness but are generally well tolerated. [2] Terbinafine is in the allylamines family of medications. [1]
Salicin from meadowsweet was used in the synthesis of aspirin (acetylsalicylic acid), [6] in 1899 by scientists at Bayer. Salicin tastes bitter like quinine. [7] Salicin may cause an allergic skin reaction (skin sensitization; category 1). [3] Mild side effects are standard, with rare occurrences of nausea, vomiting, rash, dizziness and ...
Common side effects when applied to the skin include burning, itching, and a rash. [1] Common side effects when taken by mouth include vomiting and diarrhea. [1] During pregnancy use in the vagina is safe while other formulations have not been studied in this group. [1] It works by disrupting the cell membrane of the fungal cells. [1]
Whitfield's ointment is an acidic ointment used for the topical treatment of dermatophytosis, such as athlete's foot. It can have a slight burning effect that goes away after a few minutes. It can have a slight burning effect that goes away after a few minutes.
It is synthesized by heating salicylic acid with phenol in the presence of phosphoryl chloride. [4] It also arises from heating salicylic acid: [5] 2 HOC 6 H 4 CO 2 H → C 6 H 5 O 2 C 6 H 4 OH + CO 2 + H 2 O. The conversion entails dehydration and decarboxylation. Heating phenyl salicylate in turn gives xanthone. [6] [3]
Methyl salicylate (oil of wintergreen or wintergreen oil) is an organic compound with the formula C 8 H 8 O 3.It is the methyl ester of salicylic acid.It is a colorless, viscous liquid with a sweet, fruity odor reminiscent of root beer (in which it is used as a flavoring), [4] but often associatively called "minty", as it is an ingredient in mint candies. [5]