Titanorein Lidocaine Rectal Cream 1 Tube 20 G
Symptomatic local treatment of hemorrhoidal processes that present with pain, itching, stinging or irritation.
Symptomatic local treatment of hemorrhoidal processes that present with pain, itching, stinging or irritation.
Titanorein Lidocaine (Rectal Cream 1 Tube 20 G)
ACTION AND MECHANISM
Association of local anesthetic, mucoprotector and lubricant of the anorectal mucosa. Lidocaine is an amide-type local anesthetic, which acts by blocking the propagation of the nerve impulse, by stabilizing the axoplasmic membrane of neurons. Analgesia lasts approximately 1 hour. Carrageenans (Rhodoficea extract) are lubricants that in aqueous medium produce a colloidal mucilage that lines the anorectal mucosa and facilitates evacuation.
INDICATIONS
- [HEMORROIDS]: symptomatic treatment of hemorrhoidal processes that present with pain, itching, stinging or irritation.
POSOLOGY
Topical, rectal: 1-2 applications / day, preferably in the morning, at night or after each bowel movement.
RULES FOR CORRECT ADMINISTRATION
Wash the area with a mild soap, especially after defecation, and dry without rubbing. For internal application use the cannula lubricated with the cream.
CONTRAINDICATIONS
- [ALLERGY TO LOCAL ANESTHETICS TYPE AMIDE]: Hypersensitivity to lidocaine or local anesthetics type amide (although exceptional, there is a risk of cross allergy), as well as eczema and anal itching.
PRECAUTIONS
If symptoms persist or do not improve in 7 days, consult your doctor.
- Pregnancy: there are no adequate and well-controlled studies in pregnant women.
- Lactation: Due to its low systemic absorption, it is unlikely that adverse effects will occur in the infant.
ADVICE TO THE PATIENT
- For internal use, screw the cannula onto the tube, lubricate it with the cream and gently insert it into the rectum, pressing the tube for administration.
- Wash the cannula after each application.
- If you do not improve after 7 days of continuous treatment, consult your doctor.
SPECIAL WARNINGS
- Lidocaine can interfere in tests to determine pancreatic function with bentiromide, so the medication should be suspended at least 3 days before starting the test.
ADVERSE REACTIONS
Exceptionally, pain, itching, redness, hypersensitivity reactions.
ADVERSE REACTIONS RELATING TO EXCIPIENTS
- Because it contains methyl parahydroxybenzoate, it can cause [HYPERSENSITIVITY REACTIONS] (possibly delayed).
- Because it contains propyl parahydroxybenzoate, it can cause [HYPERSENSITIVITY REACTIONS] (possibly delayed).