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MIOTENS CONTRACTURES AND DOL * SCH

  • Dompé Farmaceutici S.p.A.
  • 042045017

Miotens foam is indicated for lumbo-sciatica (back pain), cervico-brachial neuralgia (pain and contracture affecting the neck, shoulder and upper limbs), stubborn stiff necks, post-traumatic and post-operative pain syndromes.

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MIOTENS CONTRACTURES AND DOL * SCH

Therapeutic indications

Lumbo-sciatica (back pain), cervicobrachial neuralgia (pain and contracture in the neck, shoulder and upper limbs), stubborn stiff necks, post-traumatic and postoperative pain syndromes.

Dosage and method of use

Apply a quantity of foam according to the size of the area to be treated 2-3 times a day. The treatment can be associated with physical rehabilitation therapies. Method of administration : shake before use and press the dispenser while holding the container upside down.

Contraindications

Hypersensitivity to the active substance or to any of the excipients. Flaccid paralysis, muscle hypotonia. Pregnancy and lactation (see 4.6).

Side effects

Cases of rash and skin rashes have been reported. See also paragraph 4.4.

Special warnings

The dosage should be suitably reduced in case of side effects. The use, especially if prolonged, of products for topical use can give rise to sensitization phenomena. If they occur, treatment must be discontinued and appropriate therapy instituted. MIOTENS CONTRACTS AND PAIN contains propylene glycol: it can cause skin irritation.

Pregnancy and breastfeeding

Although a teratogenic effect was not observed in animal studies except when thiocolchicoside was administered at doses much higher than those recommended in human therapy (more than 10 times the therapeutic dose) as a precaution, the use of the product is contraindicated during pregnancy. Since the drug passes into breast milk, its use during breastfeeding is not recommended.

Expiration and retention

MIOTENS CONTRACTS AND PAIN 0.25% skin foam: keep away from heat. Contains flammable propellant. Do not expose to temperatures exceeding 50 ° C.

Interactions with other drugs

None known.

Overdose

Cases of overdose are not known or have been reported in the literature.

Active principles

100 ml, as a solution, contain: Active substance: thiocolchicoside 0.25 g Excipients: propylene glycol For the full list of excipients, see section 6.1

Excipients

Polysorbate 80, propylene glycol, ethyl alcohol, propylene glycol dipelargonate, benzyl alcohol, monobasic sodium phosphate monohydrate, disodium phosphate dodecahydrate, lavender Nerolene, purified water. Propellant: propane-butane mixture (propane / n-butane / iso-butane).

042045017

Data sheet

Packaging
0 -25% cutaneous foam pressurized container 30 ml
0,25% schiuma cutanea contenitore sotto pressione 30 ml
Product Type
HUMAN DRUG
ATC code
M02AX10
ATC description
Various
Therapeutic Group
Anti-inflammatories
Active principle
thiocolchicoside (DC.IT)
Class
C.
Pharmaceutical form
foam
Type of Administration
topical
Container
spray / can
Quantity
1 spray
Capacity
30 milliliters
Quantity of the Active Ingredient
2 -5MG
2.5MG
Recipe required
OTC - self-medication medicine
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