DOLOPROCT 10 suppositories
Doloproct contains glucocorticoid (Fluokortolonov pivalate) and a local anesthetic (lidocaine hydrochloride).
Fluokortolonov pivalate inhibits inflammatory and allergic skin reactions, and alleviates subjective complaints such as itching, burning and pain.
Lidocaine hydrochloride is a standard local anesthetic that is used for many years. Furthermore, it relieves pain (analgesic effect) and reduced itching (antipruritusen effect) was found to be effective when used in the form of suppositories and creams intended for the treatment of complaints in haemorrhoidal disease.
Doloprokt suppositories are used for symptomatic relief of pain, swelling, burning, itching, associated with tumors or inflammation of the rectum (proctitis).
Doloprokt can not remove the reasons for the development of haemorrhoidal disease, proctitis and anal eczema. If the hemorrhoidal disease is accompanied by inflammation and eczematous skin symptoms, it is advisable to move to the combined use of Doloprokt rectal cream and suppositories DOLOPROCT
2. BEFORE YOU USE DOLOPROCT
Do not use Doloprokt
• if you are allergic (hypersensitive) to Fluokortolonov pivalate or lidocaine hydrochloride or any of the other ingredients of Doloprokt;
• if your doctor diagnose skin infection of the affected area and if you have symptoms of these diseases in the affected area:
> Specific skin lesions (syphilis or tuberculosis);
> Reactions due to vaccination.
Take special care with DOLOPROCT
• If your doctor diagnoses that your skin disease is accompanied by a fungal infection is Expert, additional specific therapy.
• need to watch the medicinal product to avoid contact with eyes.
It is recommended after use thoroughly wash your hands.
Children and adolescents
Not recommended to treat children and adolescents as clinical trials in this age group have not been conducted.
Using other medicines
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.
If you are treated with anti-arrhythmia, lidocaine should be used with caution.
Pregnancy and lactation
Ask your doctor or pharmacist before taking any medicine.
If you are pregnant or breast-feeding, your doctor should be familiar with before prescribing Doloprokt, so please tell that you are pregnant or nursing, or that you may be pregnant.
As a rule, topical preparations containing corticosteroids should not be used during the first three months of pregnancy. In particular, should avoid prolonged use.
Driving and using machines
There are no known effects on the ability to drive and use machines.
3. HOW TO USE DOLOPROCT
Always use Doloproct cream exactly as your doctor tells you. If you're not sure, ask your doctor or pharmacist.
You should clean the anal area before you apply Doloprokt by applying it best - after defecation.
You should not use Doloproct longer than two weeks.
Unless otherwise prescribed by your doctor, it shall be the following:
Basically you can put a candle deep into the anus twice a day, morning and evening, but if complaints are strong - three times a day during the first three days. In most cases, the condition improves sufficiently only one suppository daily or every other day.
If you feel that the effect of Doloprokt is too strong or too weak, talk to your doctor or pharmacist.
If you use more than the amount Doloproct
If you use more than one dose of rectal or perianal not expect serious risk of toxicity. If the product is accepted accidental oral (eg. More than one candle), the main effects that can be expected to have systemic effects from lidocaine hydrochloride, which may occur by dose as severe cardiovascular (from weight loss to a halt cardiac) symptoms and symptoms of central nervous system (convulsions, suppression of the suspension of breathing).
If you forget to use Doloproct
Do not take a double dose to make up and continue treatment as prescribed.
If you want to stop using Doloproct
Please contact your doctor if initial symptoms of skin problems reappear.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
4. POSSIBLE SIDE EFFECTS
Like all medicines, Doloproct can cause side effects, although not everybody gets them.
The incidence of adverse reactions is determined by the data summarizing clinical study involving 367 patients. Adverse reactions are expressed only in skin irritation in the anal region with burning as common adverse reaction (> 1% to <10%) and inflammation as the most common side effects (> 0.1% and <1%).
Allergic reactions to any of the ingredients of the suppository can not be excluded.
After prolonged treatment with Doloprokt (more than four weeks) are at risk to develop local skin changes such as skin atrophy, striae or telangiectasia.
If any of the side effects gets serious, or if you notice other effects not listed in this leaflet, please tell your doctor or pharmacist.
5. HOW TO STORE DOLOPROCT
• Keep out of reach of children.
• Do not store above 30 ° C.
• Do not use Doloprokt after the expiry date stated on the packaging. The expiry date refers to the last day of that month.
• Medicines should not be disposed of in wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
6. FURTHER INFORMATION
• The active substances are: fluokortolonov pivalate and lidocaine hydrochloride.
Each suppository contains 1 mg fluokortolonov pivalate and 40 mg of lidocaine hydrochloride.
• The other ingredients are: solid mass.
How does Doloproct suppositories and contents of the pack
Doloproct suppositories are yellowish white suppositories in packs containing 6, 10 or 12 suppositories.
Not all pack sizes may be marketed.