Warticon
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS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).
The cream also contains the following excipients:
Methyl parahydroxybenzoate E218 Propyl parahydroxybenzoate E216 Sorbic acid Stearyl alcohol Cetyl alcohol
Butyl hydroxyanisole (BHA) E320 For a full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Topical cream
A homogenous white cream.
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.
Children
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.
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 cm2, 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 vagina).
Avoid applying the cream to surrounding healthy tissue.
Avoid contact with eyes. Should the cream accidentally come into the eye, the eye should be thoroughly rinsed with water and medical advice sought.
Occlusive dressings should not be used on areas treated with the cream.
Local irritation may occur on the second or third day of application associated with the start of wart necrosis. In most cases, the reactions are mild. If severe local skin reactions occur (bleeding, swelling, excessive pain, burning, itching) the cream should be washed immediately from the treatment area with mild soap and water, treatment discontinued and the patient advised to seek medical advice.
Warticon Cream is not recommended during pregnancy or in women of childbearing potential not using contraception (see section 4.6).
It is recommended that patients refrain from sexual intercourse while treating warts with the cream and until the skin has healed. If a patient does engage in sexual intercourse, a condom must be used.
This cream contains:
• methyl and propyl parahydroxybenzoate which may cause allergic reactions (possibly delayed).
• sorbic acid, stearyl alcohol and cetyl alcohol which may cause local skin reactions, (e.g. contact dermatitis).
• butyl hydroxyanisole which may cause local skin reactions (e.g.contact dermatitis), or irritation to the eyes and mucous membranes.
4.5 Interaction with other medicinal products and other forms of interaction
None presently known.
4.6. Fertility, pregnancy and lactation
Pregnancy
There are limited data from the use of podophyllotoxin in pregnant women.
Although there is very limited systemic absorption from topically applied podophyllotoxin, antimitotic products such as podophyllotoxin are known to be embryotoxic. Warticon Cream is not recommended during pregnancy or in women of childbearing potential not using contraception.
Breastfeeding
There is insufficient information on the excretion of topically applied podophyllotoxin in human milk.
A risk to the newborns/infants cannot be excluded.
A decision must be made whether to discontinue breastfeeding or to discontinue/abstain from podophyllotoxin therapy taking into account the benefit of breastfeeding for the child and the benefit of therapy for the woman.
4.7 Effects on ability to drive and use machines
None presently known.
4.8. Undesirable effects
The frequency of adverse reactions listed below is defined using the following convention: very common (> 1/10); common (> 1/100, < 1/10); uncommon (>
1/1,000, < 1/100); rare (> 1/10,000, < 1/1,000); very rare (< 1/10,000); not known (cannot be estimated from the available data). Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.
Skin and subcutaneous tissue disorders
Very Common: Skin erosion, application site irritation (including erythema, pruritus, skin burning sensation)
Post-marketing data
The following adverse drug reactions are based on post-marketing reports. Since these reports are from a population of uncertain size and are subject to confounding factors, it is not possible to reliably estimate their frequency, however in reality systemic reactions are rarely seen.
Immune system disorders
Not known: Application site hypersensitivity
Skin and subcutaneous tissue disorders
Not known: Skin ulcer, scab, skin discoloration, blister, dry skin
General disorders and administration site conditions
Not known: Application site pain, swelling, application site bleeding
Injury, poisoning and procedural complications
Not known: Caustic injury, excoriation, wound secretion
4.9. Overdose
While serious systemic effects have not been reported with the recommended dosage of topical podophyllotoxin, topical overdosage would be expected to increase systemic absorption of the drug and increase the potential for systemic effects, e.g. altered mental state and bone marrow suppression. Following oral ingestion, podophyllotoxin may also cause severe gastroenteritis.
Treatment
If topical overdosage occurs, podophyllotoxin should be washed immediately from the treatment area and symptomatic and supportive therapy initiated.
Treatment of oral podophyllotoxin poisoning is symptomatic and should include supportive care.
Further management should be as clinically indicated or as recommended by the National Poisons Centre, where available.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmaco-therapeutic group, D06BB antivirals
Podophyllotoxin is a metaphase inhibitor in dividing cells binding to at least one binding site on tubulin. Binding prevents tubulin polymerisation required for microtubule assembly. At higher concentrations, podophyllotoxin also inhibits nucleoside transport through the cell membrane.
The chemotherapeutic action of podophyllotoxin is assumed to be due to inhibition of growth and the ability to invade the tissue of the viral infected cells.
5.2. Pharmacokinetic properties
Systemic absorption of podophyllotoxin after topical application of 100 mg of 0.3% cream or 100 p,L of 0.5% solution has been studied (extravaginally in 10 females, and within the preputial cavity in 10 males, each on 2 occasions separated by 8 hours). Cmax was at or below 4.7 ng/mL following all doses and Tmax ranged from 0.5 to 36 hrs; in some subjects concentrations were below the limit of detection. The Cmax and Tmax were comparable for the 0.3% cream and 0.5% solution in both males and females. It can be concluded that systemic absorption of recommended doses of podophyllotoxin cream or solution is expected to be low.
5.3. Preclinical safety data
Carcinogenesis/Mutagenesis
Podophyllotoxin was not carcinogenic following dietary administration up to 0.3 mg/kg/day for 104 weeks in rats and 80 weeks in mice.
Podophyllotoxin was not mutagenic in in vitro Ames Assays, mouse lymphoma assay, and human lymphocyte metaphase assay. Podophyllotoxin showed evidence of mutagenicity in in vitro HPRT mutation assays, however results were inconsistent with regard to the dose response observed across replicate cultures. In mouse micronucleus studies, results were also inconsistent as one study did not show evidence of mutagenicity and one study did show evidence of an aneugenic effect (increased incidence of micronucleated polychromatic erythrocytes, mitotic arrest). Podophyllotoxin did induce aneuploidy in hamster oocytes.
Reproductive toxicology Fertility
In a multi-generational rat fertility and general reproductive performance study, podophyllotoxin administered orally up to 2.5 mg/kg/day had no effect on fertility in female or male rats.
Pregnancy
Podophyllotoxin was not teratogenic in rabbits administered up to 0.5% podophyllotoxin topically or in rats administered up to 5 mg/kg/day intraperitoneally.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Purified Water
Methyl parahydroxybenzoate E218
Propyl parahydroxybenzoate E216
Sorbic acid
Phosphoric acid
Stearyl alcohol
Cetyl alcohol
Isopropyl myristate
Paraffin, liquid
Triglycerides, medium chain
Butyl hydroxyanisole (BHA) E320
Macrogol -7 stearyl ether Macrogol - 10 stearyl ether
6.2 Incompatibilities
None known
6.3 Shelf life
3 years
6.4 Special precautions for storage
This medicinal product does not require any special storage conditions.
6.5 Nature and contents of container
A collapsible aluminium tube with imperforate nozzle membrane and internally coated with a protective lacquer. Tube cap of polyethylene with a spike on the upper end aimed to perforate the membrane when opening the tube for the first time. Size 5g and l0g.
6.6 Special precautions for disposal
No special requirements.
7 MARKETING AUTHORISATION HOLDER
GlaxoSmithKline UK Limited
980 Great West Road
Brentford
Middlesex
TW8 9GS
Trading as Stiefel Stockley Park West Uxbridge Middlesex UB11 1BT
MARKETING AUTHORISATION NUMBER(S)
PL 19494/0073
9
10
DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
26/04/1999
DATE OF REVISION OF THE TEXT
04/07/2013