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  • CDSCO Panel denies...

CDSCO Panel denies approval to Clobetasol Terbinafine Ofloxacin and Paraben FDC

MD BureauWritten by MD Bureau Published On 2021-02-04T17:48:20+05:30  |  Updated On 4 Feb 2021 5:48 PM IST
CDSCO Panel denies approval to Clobetasol Terbinafine Ofloxacin and Paraben FDC
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New Delhi: Following the justification presented by the Akums Drugs, the Central Drugs Standard Control Organization (CDSCO) Committee denied approval to the proposed Fixed-Dose Combination (FDC) of Clobetasol Terbinafine Ofloxacin and Paraben.

The Subject Expert Committee (SEC), operative under CDSCO, refused to grant permission to the firm regarding the FDC of Clobetasol Propionate 0.0500 % w/w +Terbinafine Hydrochloride 1.0000 % w/w + Ofloxacin 0.7500 % w/w + propyl Paraben 0.0200 % w/w +Methyl Paraben 0.2000% w/w cream.

Clobetasol propionate belongs to the class of steroids known as Corticosteroids. Applied to the skin as a cream, ointment, or shampoo, this drug helps get some relief from redness, itching, swelling, or other discomfort caused by certain skin conditions. The drug is known to be effective in the treatment of eczema, contact dermatitis, seborrheic dermatitis, and psoriasis.

Also Read:CDSCO Panel Gives Conditional nod to Azelnidipine and Olmesartan FDC

Terbinafine is an antifungal medication and it is also used in the treatment of certain skin conditions including pityriasis versicolor, fungal nail infections, etc.

Ofloxacin belongs to the class of antibiotics treating bacterial infections. Its common usages include pneumonia, cellulitis, urinary tract infections, prostatitis, plague, diarrhea, etc.

Propylparaben is an n-propyl ester of p-hydroxybenzoic acid. Methylparaben, on the other hand, is the methyl ester of p-hydroxybenzoic acid. Both are preservatives and are known for their usages in cosmetic and personal care products including creams, lotions, and shampoos.

In light of earlier recommendations of the committee dated 05.08.2020, the firm presented justification for the proposed FDC of Clobetasol Propionate 0.0500 % w/w +Terbinafine Hydrochloride 1.0000 % w/w + Ofloxacin 0.7500 % w/w + propyl Paraben 0.0200 % w/w +Methyl Paraben 0.2000% w/w cream.

The SEC committee in n its 54th meeting held on 12.01.2021 at CDSCO HQ New Delhi discussed all the Dermatology & Allergy related proposals and made some recommendations regarding the same.

After detailed deliberation, the committee opined that the firm did not present any additional information in support of the FDC. Committee also noted that FDC of Clobetasol+ Terbinafine + Ofloxacin + Ornidazole was prohibited.

The Committee further opined that-

1. There is no therapeutic justification/study advocating for combining the three drugs in this FDC.

2. The proposed FDC is not recommended in any standard therapeutic guidelines.

3. The proposed FDC is not approved internationally.

4. The proposed FDC may result in the emergence of bacterial and fungal resistance. Further, patients may also be unnecessarily exposed to adverse effects of potent steroids.

In view of the above, the committee did not recommend for the proposed FDC.

Also Read:Vivimed Labs gets approval for 3 ophthalmic, 3 oral liquid suspension products

CDSCO Committeecdscosec committeeclobetasol propionateTerbinafine HydrochlorideOfloxacinParabenfdc
MD Bureau
MD Bureau

    Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers.  Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in.

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