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← New search | Clotrimazole, topical

INN monograph

Clotrimazole, topical

Azole Antifungal [EPC] · POM

POM Source-linked Grade perfect

Source-linked · Updated 03 Aug 2026 · Source: Local active-ingredient clinical extract; FDA drug label via OpenFDA/DailyMed; Professional class pharmacology (Antifungal)

Kenya market

Wholesale / list prices where loaded

From
KES 262
Median
KES 262
Brands
2

Risk first

Contraindications

  • CONTRAINDICATIONS Clindamycin phosphate topical lotion is contraindicated in individuals with a history of hypersensitivity to preparations containing clindamycin or lincomycin, a history of regional enteritis or ulcerative colitis, or a history of antibiotic-associated colitis.

Precautions

  • WARNINGS Orally and parenterally administered clindamycin has been associated with severe colitis which may result in patient death.
  • Use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface.
  • Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin.
  • Studies indicate a toxin(s) produced by clostridia is one primary cause of antibiotic-associated colitis.
  • The colitis is usually characterized by severe persistent diarrhea and severe abdominal cramps and may be associated with the passage of blood and mucus.
  • Endoscopic examination may reveal pseudomembranous colitis.
  • Stool culture for Clostridium difficile and stool assay for C. difficile toxin may be helpful diagnostically.
  • When significant diarrhea occurs, the drug should be discontinued.
  • Large bowel endoscopy should be considered to establish a definitive diagnosis in cases of severe diarrhea.
  • Antiperistaltic agents such as opiates and diphenoxylate with atropine may prolong and/or worsen the condition.
  • Vancomycin has been found to be effective in the treatment of antibiotic-associated pseudomembranous colitis produced by Clostridium difficile .
  • The usual adult dosage is 500 milligrams to 2 grams of vancomycin orally per day in three to four divided doses administered for 7 to 10 days.

Point of care

Dosing

Adult

Directions • Wash the affected area and dry thoroughly. ● Apply a thin layer of this product over affected area twice daily (morning and night), or as directed by a doctor. ● Supervise children in the use of this product. ● For athlete’s foot, pay special attention to the spaces between the toes; wear well-fitting ventilated shoes, and change shoes and socks at least once daily. ● For athlete’s foot and ringworm, use daily for 4 weeks. For jock itch, use daily for 2 weeks. ● If conditions persists longer, consult a doctor. ● This product is not effective on the scalp or nails.

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Fluconazole dose-adjust in CKD; amphotericin nephrotoxicity high-alert.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.

Hepatic

Monitor LFTs for courses >14 days or higher-risk patients.

Safety

Drug interactions

Open checker →
  • Match agent to site and species.
  • For tinea, continue topical beyond clearance.
  • Invasive fungal disease needs ID/specialist input and source control.

Safety

Adverse effects

  • ADVERSE REACTIONS In 18 clinical studies of various formulations of clindamycin phosphate using placebo vehicle and/or active comparator drugs as controls, patients experienced a number of treatment emergent adverse dermatologic events [see table below].
  • Number of Patients Reporting Events Treatment Emergent Adverse Event Solution n=553(%) Gel n=148(%) Lotion n=160(%) Burning 62 (11) 15 (10) 17 (11) Itching 36 ( 7) 15 (10) 17 (11) Burning/Itching 60 (11) # ( – ) # ( – ) Dryness 105 (19) 34 (23) 29 (18) Erythema 86 (16) 10 ( 7) 22 (14) Oiliness/Oily Skin 8 ( 1) 26 (18) 12* (10) Peeling 61 (11) # ( – ) 11 ( 7) # not recorded * of 126 subjects Orally and parenterally administered clindamycin has been associated with severe colitis which may end fatally.
  • Cases of diarrhea, bloody diarrhea and colitis (including pseudomembranous colitis) have been reported as adverse reactions in patients treated with oral and parenteral formulations of clindamycin and rarely with topical clindamycin (see WARNINGS ).
  • Abdominal pain, gastrointestinal disturbances, gram-negative folliculitis, eye pain and contact dermatitis have also been reported in association with the use of topical formulations of clindamycin.
  • To report SUSPECTED ADVERSE REACTIONS, contact Perrigo at 1-866-634-9120 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .

Use

Indications

  • INDICATIONS AND USAGE Clindamycin phosphate topical lotion is indicated in the treatment of acne vulgaris.
  • In view of the potential for diarrhea, bloody diarrhea and pseudomembranous colitis, the physician should consider whether other agents are more appropriate (see CONTRAINDICATIONS , WARNINGS and ADVERSE REACTIONS ).

Pharmacology

Mode of action

Mechanism of Action The mechanism of action of clindamycin in treating acne vulgaris is unknown.

Mechanism of Action The mechanism of actio… Azoles inhibit fungal CYP51 (lanosterol 14… Terbinafine inhibits squalene epoxidase.
Full mechanism text

Mechanism of Action The mechanism of action of clindamycin in treating acne vulgaris is unknown. Azoles inhibit fungal CYP51 (lanosterol 14α-demethylase), depleting ergosterol and disrupting membrane integrity. Terbinafine inhibits squalene epoxidase. Polyenes bind ergosterol creating membrane pores. Echinocandins inhibit β-glucan synthase (cell wall).

ADME

Pharmacokinetics & PD

Onset Days for clinical response (varies)
Duration Days–weeks per indication
Route ORAL / TOPICAL / IV
Full PK/PD text

Pharmacokinetics Following multiple topical applications of clindamycin phosphate at a concentration equivalent to 10 mg clindamycin per mL in an isopropyl alcohol and water solution, very low levels of clindamycin are present in the serum (0–3 ng/mL) and less than 0.2% of the dose is recovered in urine as clindamycin. Although clindamycin phosphate is inactive in vitro , rapid in vivo hydrolysis converts this compound to the antibacterially active clindamycin.

Kenya

Brands & prices

2 listed
Brand Company Pack KES
CANDID CREAM * DAIMA BIASHARA / Wholesale Import 20GM 264.07
CANDID POWDER * DAIMA BIASHARA / Wholesale Import 30GM 262.25

Special populations

Pregnancy & lactation

Pregnancy

Pregnancy: Teratogenic effects In clinical trials with pregnant women, the systemic administration of clindamycin during the second and third trimesters has not been associated with an increased frequency of congenital abnormalities. There are no adequate studies in pregnant women during the first trimester of pregnancy. Clindamycin should be used during the first trimester of pregnancy only if clearly needed.

Lactation

Nursing Mothers It is not known whether clindamycin is excreted in breast milk following use of clindamycin phosphate. However, orally and parenterally administered clindamycin has been reported to appear in breast milk. Clindamycin has the potential to cause adverse effects on the breast-fed infant's gastrointestinal flora. Monitor the breast-fed infant for possible adverse effects on the gastrointestinal flora, such as diarrhea, candidiasis (thrush, diaper rash) or rarely, blood in the stool indicating possible antibiotic-associated colitis. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for clindamycin and any potential adverse effects on the breast-fed child from clindamycin or from the underlying maternal condition. Clinical Considerations If used during lactation and clindamycin phosphate topical lotion is applied to the chest, care should be taken to avoid accidental ingestion by the infant.

Diet

Food & alcohol

  • Food
  • Food

Trust

Sources & disclaimer

Source: Local active-ingredient clinical extract; FDA drug label via OpenFDA/DailyMed; Professional class pharmacology (Antifungal)

Open source link

Clinical review date not recorded.

Decision support only — not a substitute for clinical judgment, product SmPC, or Kenya STG/EML.

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