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- FASTUM GEL 2.5% [SIN06755P]
FASTUM GEL 2.5% [SIN06755P]
Active ingredients: FASTUM GEL 2.5%
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Product Info
FASTUM GEL 2.5%
[SIN06755P]
Product information
Active Ingredient and Strength | KETOPROFEN - 2.5 G/100 G |
Dosage Form | GEL |
Manufacturer and Country | A. MENARINI MANUFACTURING LOGISTICS AND SERVICES S.R.L. - ITALY |
Registration Number | SIN06755P |
Licence Holder | A. MENARINI SINGAPORE PTE. LTD. |
Forensic Classification | PHARMACY ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | M02AA10 |
INDICATIONS
Painful, phlogistic or traumatic affections of the joints, tendons, ligaments and muscles (arthritis, periarthritis, arthrosynovitis, tendinitis, tenosynovitis, bursitis, contusions, sprains, luxations, lesions of the knee's meniscus, torticollis, lumbago). Phlebitis, periphlebitis, lymphoangitis, superficial lymphoadenitis. Erythemas and cutaneous phlogistic processes.
DOSAGE AND ADMINISTRATION
Apply a thin layer of gel on the area of affected skin, once or twice a day, gently massaging to help absorption.
Opening of the soft tube: unscrew the cap and perforate the diaphragm of aluminium with the point of the inverted cap.

Pre-filling of the dispensing tube: push the dispenser cap several times or push the base of the tube until the gel appears; it is advisable to use it in a horizontal position.

Consult your physician in case of allergic or other kind of skin reactions.
Seek your physician's advice if the condition occurs repeatedly or if you have noted any kind of recent change in its characteristics.
Caution: do not exceed recommended doses without consulting your physician. Use only for brief periods of treatment
Paediatric population
The safety and efficacy of ketoprofen gel in children have not been established.
CONTRAINDICATIONS
History of hypersensitivity to the active substance or to any of the excipients included in section “Composition” – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information
History of any photosensitivity reactions.
Known hypersensitivity reactions, such as asthma symptoms, allergic rhinitis to ketoprofen, fenofibrate, tiaprofenic acid, acetylsalicylic acid or other NSAIDs.
History of skin allergy to ketoprofen, tiaprofenic acid, fenofibrate, UV blockers or parfumes.
Sun exposure, even in case of hazy sun, including UV light from solarium, during the treatment and 2 weeks after its discontinuation (see section “Special warning and precautions for use” – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Application on pathological skin changes such as eczema or acne; in Infectious skin or open wounds.
Third trimester of pregnancy (see section "Use in Pregnancy and Breastfeeding" – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
