Descrizione Clinica
Hemorrhoids Proctosoll cream rett 30g otc Proctosoll
PROCTOSOLL “CREAM RETTALE”
active ingredients
g 100 of cream cream cream contain: - BENZOCAINA g: 5; - IDROCORTISONE ACETATO g: 0.5; - EPARINA SODICA U.I: 5.000. For excipients, see 6.1.
Excellent
Cetostearilic alcohol, isopropylmiristato, gGlicole propilenico, macrogol cetostearil ether, dimeticone, isotiazolinone, levomentolo, EDTA disodium, butilidroxyanisolo, purified water.
Therapeutic indications
Syntomatic treatment of uncomplicated external hemorrhoids.
Contraindications
Hypersensitivity to components or other substances closely related to chemical. Skin injuries of tubercular nature. Viral infections.
Population
In acute forms, especially after evacuation, apply the cream 2-3 times a day. Do not exceed the recommended doses.
Conservation
Store at temperature not exceeding 30 ° C.
Warnings
After a short period of treatment, without appreciable results, consult your doctor. Excessive application and/or for prolonged periods of cortisonic can give rise to generalized reactions from systemic absorption. The use, especially if prolonged, of products for topical use can give rise to awareness-raising phenomena. In this case it is necessary to stop treatment and establish suitable therapy. The effectiveness and safety of benzocaine depend on a correct dosage; it is therefore necessary to use the minimum quantity of the preparation sufficient to obtain the desired effect by applying it with caution in subjects with severely damaged mucosa or home to inflammatory processes that could cause excessive absorption of the active ingredient. A high absorption of benzocaine can provide severe reactions in particular in children and elderly patients. Proctosoll contains propylene glycol This medicine contains 25 mg of propylene glycol per dose equivalent to 25 mg /g. Proctosoll contains butilidroxyanisolo It can cause reactions to localized skin (e.g. contact dermatitis) or irritation to the eyes and mucosa. Proctosoll contains cetostearilic alcohol It can cause reactions to localized skin (e.g. contact dermatitis). Keep the medicine out of reach of children.
Interactions
Particular attention in use must be observed in conjunction with other anticoagulant treatments.
Effects
Locally they can manifest themselves, sometimes, sense of burning, irritation, dryness of the skin, follicles, acne eruptions, hypertricosis, hyperpigmentation and skin atrophy. At the eventual appearance of some local reaction typical of corticotherapy, you can avoid suspending treatment.Reporting of suspicious adverse reactions The reporting of suspicious adverse reactions that occur after the authorization of the medicinal product is important, as it allows continuous monitoring of the benefit/risk ratio of the medicinal product. Healthcare workers are required to report any suspected adverse reaction via the national reporting system at the address https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse.
Overdosing
No known overdose symptoms.
In pregnant women the use must be carried out only in case of actual need and under the direct control of the doctor.
Source: Farmadati
