Condylox Topical Solution 0.5pct Drug Medication Dosage Information
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Condylox: Topical solution (0.5%)

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What is this Medicine?

PODOFILOX (po do FIL ox) is a medication used to remove genital warts. The topical solution should only be used to treat genital warts located on the outside skin of the genitals (i.e., penis or vagina). The solution should not be used to treat warts near the rectal area.

Similar Generic Drugs : Podofilox: Topical solution (0.5%)
In-Depth Information
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Condylox 0.5% Topical Solution

NDC: 525440046
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Condylomata Acuminata, Human Papillomavirus (HPV) Infection

Storage Information
Store at room temperature (between 59 to 86 degrees F)
Protect from freezing
Avoid excessive heat (above 104 degrees F)
Condylox 0.5% Topical Solution

Reported Side Effects for Condylox 0.5% Topical Solution

Upset Stomach Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Skin Ulcer Incidence:
<5.0%*
Severity: MODERATE
Onset: DELAYED
Skin Ulcer Incidence:
<67.0%*
Severity: MODERATE
Onset: DELAYED
Skin Discoloration Incidence:
<5.0%*
Severity: MILD
Onset: DELAYED
Skin Rash Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Phimosis Incidence:
<5.0%*
Severity: SEVERE
Onset: DELAYED
Painful Intercourse Incidence:
<5.0%*
Severity: MODERATE
Onset: DELAYED
Lightheadedness Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Blood In The Urine Incidence:
<5.0%*
Severity: MODERATE
Onset: DELAYED
Bleeding Incidence:
<19.0%*
Severity: MODERATE
Onset: EARLY
Dry Skin Incidence:
<5.0%*
Severity: MILD
Onset: DELAYED
Itching Incidence:
<65.0%*
Severity: MILD
Onset: RAPID
Inability To Sleep Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Swelling Incidence:
<5.0%*
Severity: MODERATE
Onset: DELAYED
Skin Redness Incidence:
5.0%*
Severity: MODERATE
Onset: EARLY
Headache Incidence:
7.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


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