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Aldara
Eintrag öffnenAldara · 4.1 Therapeutic indications · 1
Eintrag öffnenAldara · 4.3 Contraindications · 1
Eintrag öffnenAldara · 4.3 · Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Eintrag öffnenAldara · 4.4 Special warnings and precautions for use · 1
Eintrag öffnenAldara · 4.5 Interaction with other medicinal products and other forms of interaction · 1
Eintrag öffnenAldara · 4.5 · Due to its immunostimulating properties, imiquimod cream should be used with caution in patients who are recei
Eintrag öffnenAldara · 4.5 · No interaction studies have been performed. This includes studies with immunosuppressive drugs. Interactions w
Eintrag öffnenAldara · 4.6 Fertility, pregnancy and lactation · 1
Eintrag öffnenAldara · 4.8 Undesirable effects · 1
Eintrag öffnenAldara · 4.8 · 8 Respiratory, thoracic and mediastinal disorders: Pharyngitis Uncommon Rhinitis Uncommon Nasal congestion Unc
Eintrag öffnenAldara · 4.8 · 9 Application site bleeding Common Uncommon Application site papules Common Uncommon Application site paraesth
Eintrag öffnenAldara · 4.8 · Clinical studies investigating the use of imiquimod for the treatment of actinic keratosis have detected a 0.4
Eintrag öffnenAldara · 4.8 · External genital Superficial basal Actinic keratosis warts cell carcinoma (3x/ wk,16wks) (5x/wk, 6 wks) (3x/wk
Eintrag öffnenAldara · 4.8 · External genital warts:
Eintrag öffnenAldara · 4.8 · Frequencies are defined as Very common (1/10), Common (1/100 to <1/10) and Uncommon (1/1,000 to <1/100). Lo
Eintrag öffnenAldara · 4.8 · Imiquimod was investigated in controlled clinical studies with paediatric patients (see sections 4.2 and 5.1).
Eintrag öffnenAldara · 4.8 · In clinical trials of imiquimod cream 3 times weekly for 4 or 8 weeks the most frequently occurring applicatio
Eintrag öffnenAldara · 4.8 · In the pivotal trials with 3 times a week dosing, the most frequently reported adverse drug reactions judged t
Eintrag öffnenAldara · 4.8 · In trials with 5 times per week dosing 58% of patients experienced at least one adverse event. The most freque
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