Jak stosować PROKTOSOLL
Treść ulotki
Proctosoll rectal cream
Benzocaine, Hydrocortisone acetate, Sodium heparin
Read this leaflet carefully before using this medicine as it contains important
information for you.
Always use this medicine exactly as described in this leaflet or as your doctor or
pharmacist has told you.
- Keep this leaflet. You may need to read it again.
- If you want more information or advice, ask your pharmacist.
- If any side effects occur, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.
- See a doctor if you do not feel better or if your symptoms get worse.
Contents of this leaflet:
- 1. What Proctosoll is and what it is used for
- 2. What you need to know before using Proctosoll
- 3. How to use Proctosoll
- 4. Possible side effects
- 5. How to store Proctosoll
- 6. Contents of the pack and other information
1. What is Proctosoll and what is it for
Proctosoll is a cream indicated in the symptomatic treatment of uncomplicated external hemorrhoids.
It is applied locally to the hemorrhoids and contains 3 active ingredients:
- Benzocaine which has the function of relieving local pain (local anesthetic).
- Hydrocortisone acetate which serves to reduce inflammation and itching.
- Sodium heparin which reduces blood coagulation (anticoagulant). The action of these active ingredients produces a reduction of the symptoms of hemorrhoids, especially in the acute phase.
2. What you need to know before using Proctosoll
DO NOT use Proctosoll
- if you are allergic to benzocaine, hydrocortisone acetate and sodium heparin or to any of the other ingredients of this medicine (listed in section 6).
- if you have skin lesions due to forms of tuberculosis.
- in case of concurrent viral infections.
Warnings and precautions
- This medicine should not be used for prolonged treatments, after a short period of treatment without appreciable results consult your doctor.
- Use the minimum amount of cream to achieve the desired effect, applying Proctosoll with caution especially in case of severe lesions or inflammation of the rectal mucosa, as excessive use can cause high absorption of the active ingredients.
- Excessive application or for prolonged periods of drugs based on cortisone can alter absorption by the body.
- High absorption of benzocaine can cause serious reactions, especially in children and the elderly.
- Discontinue treatment and consult your doctor in case of allergic reactions after prolonged use of the medicine.
- During treatment with medicines containing benzocaine, a condition known as methemoglobinemia may occur, characterized by the inability of hemoglobin to transport oxygen efficiently. The risk is greater in case of prolonged use, application of high dosages and in subjects of low body weight, such as children. If you experience symptoms such as bluish discoloration of the skin or lips (cyanosis), headache, dizziness, shortness of breath, fatigue or rapid heartbeat (tachycardia) after using Proctosoll, seek immediate medical attention, as methemoglobinemia is a serious condition, and prompt treatment is essential.
Other medicines and Proctosoll
Tell your doctor or pharmacist if you are taking, have recently taken or might take
any other medicine.
Pay particular attention in case of concomitant treatment with other medicines that reduce
blood coagulation (anticoagulants).
Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant or are planning a pregnancy, or if you are breastfeeding with
breast milk, ask your doctor or pharmacist for advice before using this medicine.
During pregnancy and breastfeeding use Proctosoll only if absolutely necessary and only after
consulting your doctor and evaluating with him the benefit-risk ratio for
the fetus or infant.
Driving and operating machinery
Proctosoll does not impair the ability to drive vehicles or operate machinery.
For athletes
The use of the drug without a medical need constitutes doping and can give positive results of doping-
control tests.
Proctosoll contains propylene glycol
This medicine contains 25 mg of propylene glycol per dose equivalent to 25 mg /g.
Proctosoll contains butylated hydroxyanisole
May cause localized skin reactions (e.g. contact dermatitis) or irritation to the eyes and
mucous membranes.
Proctosoll contains cetostearyl alcohol
May cause localized skin reactions (e.g. contact dermatitis).
3. How to use Proctosoll
Use this medicine following exactly as stated in this leaflet or as instructed by your doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
The recommended dose in acute cases is 2-3 applications per day, particularly after bowel movement (evacuation). Use the special cannula screwed onto the tube to distribute the cream.
Use the medicine only for short periods of treatment and do not exceed the indicated doses without the advice of your doctor.
If you use more Proctosoll than you should
Immediately inform your doctor or go to the nearest hospital if you have used an excessive dose of the medicine.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Locally, the following side effects may occur:
- burning or pain
- irritation
- skin dryness
- inflammation around the hair follicles (folliculitis)
- skin rash similar to acne (acneiform eruption)
- excessive hair growth (hypertrichosis)
- skin hyperpigmentation (alteration of skin color)
- skin thinning (skin atrophy)
The side effects listed above are generally transient. You should stop the
treatment and consult your doctor if any of the above local reactions occur and
are typical of therapies based on cortisone.
Reporting of side effects
If you get any side effects, even if not listed in this leaflet, tell your
doctor or pharmacist. You can also report side effects directly through the
national reporting system at https://www.aifa.gov.it/content/segnalazioni-reazioni-
avverse
By reporting side effects you can help provide more information on the safety
of this medicine.
5. How to store Proctosoll
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the packaging. The expiry date refers to the last day of that month.
Do not store at a temperature above 30 °C.
Do not use this medicine if the packaging has been opened or damaged.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to
dispose of medicines you no longer use. This will help protect the environment.
It is important to always have the information about the medicine available, therefore keep both the
6. Contents of the pack and other information
What Proctosoll contains
- The active ingredients are: Benzocaine, hydrocortisone acetate, sodium heparin. 100 g of cream contain: 5 g of benzocaine, 0.5 g of hydrocortisone acetate, 5,000 I.U. of sodium heparin.
- The other ingredients are: cetostearyl alcohol, isopropyl myristate, propylene glycol,
macrogol cetostearyl ether, dimethicone, isotiazolinone, levomenthol, disodium edetate,
butylhydroxyanisole, purified water.
Description of the appearance of Proctosoll and contents of the pack
Proctosoll is presented in the form of a rectal cream.
Each pack contains a tube with 20 or 30 grams of cream and a cannula for distributing the
cream.
Not all pack sizes may be marketed.
Marketing Authorisation Holder and Manufacturer
Marketing Authorisation Holder:
Alfasigma S.p.A. – Via Ragazzi del ‘99, n. 5 - 40133 Bologna (BO)
Manufacturer:
Alfasigma S.p.A. – Via E. Fermi, n. 1 – 65020 Alanno (PE)
Doppel Farmaceutici S.r.l. Via Martiri delle Foibe n. 1 Cortemaggiore (PC)

- Kraj rejestracji
- Postać farmaceutycznaCream, 20 g
- Kod ATCC05AA01
- Substancja czynna
- Wymaga receptyNie
- Producent
- Te treści mają charakter wyłącznie informacyjny i nie zastępują konsultacji lekarskiej.
- Zamienniki PROKTOSOLLPostać farmaceutyczna: Cream, 1% + 1.5%Substancja czynna: hydrocortisoneBez receptyPostać farmaceutyczna: Cream, 20 GSubstancja czynna: hydrocortisoneProducent: KARO HEALTHCARE ABBez receptyPostać farmaceutyczna: Rectal cream, 0,1 MG/G + 10 MG/GSubstancja czynna: fluocinolone acetonideBez recepty
Odpowiedniki PROKTOSOLL w innych krajach
Leki z tą samą substancją czynną dostępne w innych krajach.
Odpowiednik PROKTOSOLL w Hiszpania
Odpowiednik PROKTOSOLL w Polska
Odpowiednik PROKTOSOLL w Ukraina
Lekarze online w sprawie PROKTOSOLL
Omów stosowanie PROKTOSOLL, bezpieczeństwo i ocenę zasadności recepty zgodnie z obowiązującymi przepisami.
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Często zadawane pytania
PROKTOSOLL nie wymaga recepty w Włochy. Możesz skonsultować się z lekarzem online, aby sprawdzić, czy ten lek może być odpowiedni w Twojej sytuacji.
Substancją czynną w PROKTOSOLL jest hydrocortisone. Informacja ta pomaga rozpoznać leki o tym samym składzie, ale pod różnymi nazwami handlowymi.
PROKTOSOLL jest produkowany przez ALFASIGMA S.P.A.. Nazwy handlowe i opakowania mogą się różnić w zależności od dystrybutora.
Lekarze, tacy jak Lekarze rodzinni, Psychiatrzy, Dermatolodzy, Kardiolodzy, Endokrynolodzy, Gastroenterolodzy, Pulmonolodzy, Nefrolodzy, Reumatolodzy, Hematolodzy, Zakaźnicy, Alergolodzy, Geriatrzy, Pediatrzy, Onkolodzy, mogą ocenić, czy stosowanie PROKTOSOLL jest odpowiednie w Twoim przypadku, w zależności od sytuacji klinicznej i lokalnych przepisów. Możesz umówić konsultację online, aby omówić objawy i możliwe dalsze kroki.
Polska posiada dobrze rozwiniętą infrastrukturę ochrony zdrowia w dużych miastach, takich jak Warszawa, Kraków, Wrocław i Gdańsk. Apteki są łatwo dostępne i działają zgodnie z obowiązującymi przepisami, zapewniając dostęp do leków na receptę.
Możesz kupić PROKTOSOLL w Warszawie, Krakowie, Wrocławiu lub Gdańsku w każdej aptece, posiadając ważną receptę.
Aby uzyskać receptę, możesz skorzystać z Oladoctor:
Inne leki zawierające tę samą substancję czynną (hydrocortisone) to m.in. EMORRIL, PROKTOSEDYL, PROKTOLYN. Mogą one różnić się nazwą handlową lub postacią, ale zawierają ten sam składnik terapeutyczny. Przed zmianą lub rozpoczęciem nowego leku skonsultuj się z lekarzem.
















