PROSPIDOL

Description
Medical device based on plant extracts useful as an adjuvant in treatments aimed at maintaining the properties of the prostate gland or known for their beneficial properties on urinary tract functions.
It may have a beneficial effect in inflammatory prostate conditions and in actinic proctitis (induced by radiotherapy) or other types.
The product is suitable for short-term use in case of constipation and hemorrhoidal congestion due to its soothing action.

How to use
We recommend one suppository per day, preferably in the evening before bedtime. For optimal effectiveness, it is recommended to apply the suppository correctly, ensuring that it is inserted correctly into the deepest part of the rectal ampoule.

components
Lactoferrin, glycerophosphoinositol, hyaluronic acid.

warnings
The uneven dark color that the suppository may exhibit is a characteristic of the product and does not indicate deterioration in its effectiveness or improper storage.
Keep out of reach of children.
Do not use after the expiry date stated on the packaging and blister.
PROSPIDOL is not sterile; however, it is recommended not to use the suppositories if the primary packaging (blister) is damaged.
Each suppository is for single use only and should be removed from the packaging immediately before use. Do not use suppositories that have been broken or removed from the blister at an unknown time, as this could pose a risk of contamination of the product. Do not attempt to reuse suppositories that have accidentally leaked after first use.
Do not exceed the recommended dose; if DM is ineffective after proper use, according to the recommended dose, discontinue use and consult a doctor. Abuse of laxatives, especially contact laxatives (stimulant laxatives), can cause dependence, chronic constipation and loss of normal bowel function (intestinal atony), persistent diarrhea leading to loss of water, minerals (especially potassium) and other essential nutrients. In more severe cases of abuse, dehydration or hypokalemia may occur, which can lead to cardiac or neuromuscular dysfunction, especially when treated concomitantly with cardiac glycosides, diuretics or corticosteroids.
PROSPIDOL does not adversely affect sensory abilities (level of attention, ability to drive or perform activities). However, if you experience any adverse reactions, such as excessive irritation, pain or any discomfort that may occur in connection with the use of the medical device, discontinue use immediately and consult a doctor.
PROSPIDOL suppositories may reduce the residence time in the intestine and, consequently, the absorption of other drugs taken orally at the same time. Therefore, it is recommended to wait at least 2 hours after taking an oral drug before taking PROSPIDOL. However, whenever possible, avoid taking PROSPIDOL while using other devices or drugs. Consult your doctor before taking PROSPIDOL if you are currently taking other drugs.
Do not use in children under 12 years of age.
The administration of PROSPIDOL is not recommended in case of known hypersensitivity of the user to one of the components.
Do not use if:
- acute or unknown abdominal pain;
- nausea or vomiting;
- intestinal obstruction or stenosis;
- rectal bleeding of unknown origin;
- acute hemorrhoidal crisis with pain and bleeding;
- severe dehydration.
PROSPIDOL can be used during pregnancy or breastfeeding, but only in cases of real need and only after consulting a doctor.
Elderly or unhealthy people should consult their doctor before using PROSPIDOL.

Conservation
Store in a dry place, away from direct light or heat. Remove the suppository only immediately before use. Store below 25°C.
Shelf life in intact packaging: 24 months.

Format
10 suppositories of 2 g each