Valsts: Lielbritānija
Valoda: angļu
Klimata pārmaiņas: MHRA (Medicines & Healthcare Products Regulatory Agency)
Podophyllotoxin
DE Pharmaceuticals
D06BB04
Podophyllotoxin
1.5mg/1gram
Cutaneous cream
Cutaneous
No Controlled Drug Status
Valid as a prescribable product
BNF: 13070000
PATIENT INFORMATION LEAFLET WARTICON® 0.15% W/W CREAM (podophyllotoxin) READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. • Keep this leaflet. You may need to read it again. • If you have any further questions, ask your doctor or pharmacist. • This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. • If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. The name of your medicine is Warticon 0.15% w/w Cream, but will be referred to as Warticon Cream throughout the remainder of the leaflet. WHAT IS IN THIS LEAFLET: 1. What Warticon Cream is and what it is used for 2. What you need to know before you use Warticon Cream 3. How to use Warticon Cream 4. Possible side effects 5. How to store Warticon Cream 6. Contents of the pack and other information 1. WHAT WARTICON CREAM IS AND WHAT IT IS USED FOR Warticon Cream contains a medicine called podophyllotoxin. This is a plant extract which belongs to a group of medicines called ‘antivirals’. Warticon Cream is used to treat genital warts. It is used for warts on the penis in men or external warts on the vagina in women. 2. WHAT YOU NEED TO KNOW BEFORE YOU USE WARTICON CREAM DO NOT USE WARTICON CREAM IF: • you are ALLERGIC (_hypersensitive_) to podophyllotoxin or any of the other ingredients of Warticon Cream (listed in Section 6) • your warts are on areas of broken/damaged or bleeding skin • you are already using another medicine containing podophyllotoxin. WARNINGS AND PRECAUTIONS Talk to your doctor or pharmacist before using this medicine if: • your warts cover an area bigger than 4 centimetres (approximately the size of a postage stamp). You may need to have this medicine applied by a nurse/doctor in a clinic. WARTICON CREAM IS ONLY TO BE USED ON THE AFFECTED SKIN. Do not take Warticon Cream by mout Izlasiet visu dokumentu
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Warticon 0.15% w/w Cream 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Podophyllotoxin 1.5 mg/g (0.15% w/w). Excipients with known effect: Methyl parahydroxybenzoate (E218) 0.100 %w/w Propyl parahydroxybenzoate (E216) 0.030 %w/w Sorbic acid 0.120 %w/w Stearyl alcohol 2.000 %w/w Cetyl alcohol 2.000 %w/w Butyl hydroxyanisole (BHA) (E320) 0.015 %w/w For the full list of excipients, see section 6.1 3 PHARMACEUTICAL FORM Topical cream A homogenous white cream. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS _ _ _Route of administration: Topical _ For the topical treatment of condylomata acuminata affecting the penis or the external female genitalia. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION The affected area should be thoroughly washed with soap and water, and dried prior to application. Using a fingertip, the cream should be applied twice daily morning and evening (every 12 hours) for 3 consecutive days using only enough cream to just cover each wart. The cream should then be withheld for the next 4 consecutive days. Application to the surrounding normal tissue should be avoided. Residual warts should be treated with further courses of twice daily applications for three days at weekly intervals, if necessary for a total of 4 weeks of treatment. Hands should be washed thoroughly after application. _Paediatric population _ The safety and efficacy of topical podophyllotoxin have not been established in children under the age of 18. 4.3 CONTRAINDICATIONS Hypersensitivity to the active substance or to any of the excipients listed in section 6.1. Open or bleeding wounds. Concomitant use with other podophyllotoxin containing preparations. 4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE Where the area of treatment is greater than 4 cm 2 , it is recommended that treatment takes place under the direct supervision of a healthcare professional. Avoid applying the cream to warts occurring on mucous membranes of the genital area (including the urethra, rectum and vagi Izlasiet visu dokumentu