Clindamycin + Benzoyl peroxide interactions
Checked as Clindamycin + Benzoyl peroxide (topical) in this data source.
Full monograph for Clindamycin + Benzoyl peroxideCheck it against another medicine
Medicines
437 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Abametapirvia Clindamycin | Moderate | Metabolism | Based on in vitro inhibition data, a single topical application of abametapir lotion may increase plasma concentrations of drugs that are substrates of CYP450… | 1 sources — open the full entry |
| Apalutamidevia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inducers may decrease plasma concentrations and antimicrobial effects of clindamycin, which is metabolized… | 6 sources — open the full entry |
| Atracurium Besilatevia Clindamycin | Moderate | Synergy | Lincosamides (e.g., clindamycin, lincomycin) have demonstrated neuromuscular blocking activity in vitro and may augment the pharmacologic effects of… | 13 sources — open the full entry |
| Bacitracin Zinc + Polymyxin B Sulfatevia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| Betamethasone + Clotrimazole + Gentamicinvia Clindamycin | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly…2 documented mechanisms | 2 sources — open the full entry |
| Carbamazepinevia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inducers may decrease plasma concentrations and antimicrobial effects of clindamycin, which is metabolized… | 6 sources — open the full entry |
| Ceritinibvia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Cisatracurium Besylatevia Clindamycin | Moderate | Synergy | Lincosamides (e.g., clindamycin, lincomycin) have demonstrated neuromuscular blocking activity in vitro and may augment the pharmacologic effects of… | 13 sources — open the full entry |
| Clarithromycinvia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Clascoteronevia Benzoyl peroxide (topical) | Moderate | Synergy | Clascoterone applied topically can cause local irritation such as erythema or redness, pruritus, scaling, and dryness. Concomitant use with other potentially… | 1 sources — open the full entry |
| Colistimethate Sodiumvia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Cyclosporine (Oral)via Clindamycin | Moderate | Others | Cyclosporine plasma concentrations may be reduced during coadministration with oral clindamycin. The mechanism is unknown. | 14 sources — open the full entry |
| Cyproterone Acetate + Ethinyl Estradiolvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Dexamethasone + Neomycin Sulphate + Polymyxin B Sulphatevia Clindamycin | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| Dienogest + Estradiol Valeratevia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Drospirenone + Estradiolvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol0.02 mg0.03 mgvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol + Levomefolatevia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Enzalutamidevia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inducers may decrease plasma concentrations and antimicrobial effects of clindamycin, which is metabolized… | 6 sources — open the full entry |
| ErythromycinLotionOralvia Clindamycin | Moderate | Distribution | Lincomycin derivatives and erythromycin have antagonistic effects in vitro. The mechanism is competitive binding of the 50S ribosomal subunit. | 9 sources — open the full entry |
| Esomeprazole + Amoxicillin + Clarithromycinvia Clindamycin | Moderate | Metabolism · Unknown | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized…2 documented mechanisms | 2 sources — open the full entry |
| Estradiolbasevaginal creamvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiol + Dydrogesteronevia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiol Hemihydrate + Progesterone Micronizedvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Estradiol Valeratevia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Desogestrel0.02 mg0.03 mgvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Gestodenevia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Levonorgestrel + Ferrous Fumaratevia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Ethinyl Estradiol + Lynestrenol0.0375 mg0.05 mgvia Clindamycin | Moderate | Antagonism | RECOMMENDED: The effectiveness of estrogen-containing oral contraceptives may be impaired by concomitant treatment with antimicrobial agents. Most… | 38 sources — open the full entry |
| Fluorometholone + Gentamicinvia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Fosphenytoin Sodiumvia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inducers may decrease plasma concentrations and antimicrobial effects of clindamycin, which is metabolized… | 6 sources — open the full entry |
| Gentamicin + Hydrocortisone Acetatevia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Gentamicin SulfateInjectionOphthalmicvia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. Patients who are elderly… | 2 sources — open the full entry |
| Gramacidin + Neomycin + Polymixin Bvia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Hydrocortisone + Neomycin Sulphate + Polymixin Bvia Clindamycin | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| IsotretinoinOralTopicalvia Benzoyl peroxide (topical) | Moderate | Synergy | Concomitant use of isotretinoin with topical exfoliative or keratolytic anti-acne agents may increase local skin irritation. | 2 sources — open the full entry |
| Itraconazolevia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Ketoconazolevia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Ketoconazole + Zinc Pyrithione + Aleoveravia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Lactobacillus Rhamnosus GGvia Clindamycin | Moderate | Antagonism | Coadministration of oral probiotic preparations with oral antibiotics may reduce the efficacy of the probiotic. It has been theorized that concomitant… | 1 sources — open the full entry |
| Lansoprazole + Amoxicillin + Clarithromycinvia Clindamycin | Moderate | Metabolism · Unknown | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized…3 documented mechanisms | 2 sources — open the full entry |
| Lopinavir + Ritonavirvia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Metronidazole + Neomycin Sulphate + Polymyxin B + Nystatinvia Clindamycin | Moderate | Synergy · Unknown | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.3 documented mechanisms | 2 sources — open the full entry |
| Mycophenolate Mofetilvia Clindamycin | Moderate | Absorption | Theoretically, drugs that alter the gastrointestinal flora (e.g., antibiotics) may reduce the oral bioavailability of mycophenolic acid products. Some… | 3 sources — open the full entry |
| Mycophenolic acidvia Clindamycin | Moderate | Absorption | Theoretically, drugs that alter the gastrointestinal flora (e.g., antibiotics) may reduce the oral bioavailability of mycophenolic acid products. Some… | 3 sources — open the full entry |
| Nelfinavirvia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
| Neomycin Sulfate + Bacitracin Zincvia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Neomycin Sulfate + Bacitracin Zinc + Polymyxin B Sulfatevia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity.2 documented mechanisms | 2 sources — open the full entry |
| Neomycin Sulphate + Polymyxin B Sulphate + Pramoxinevia Clindamycin | Moderate | Synergy | The concurrent or sequential use of two or more potentially nephrotoxic or neurotoxic drugs may increase the risk of toxicity. | 2 sources — open the full entry |
| Nirmatrelvir + Ritonavirvia Clindamycin | Moderate | Metabolism | Coadministration with strong CYP450 3A4 inhibitors may increase plasma concentrations and the risk of adverse effects of clindamycin, which is metabolized… | 2 sources — open the full entry |
Conditions
Conditions in which Clindamycin + Benzoyl peroxide needs care, as documented in this source.
Colitis
MajorClostridioides difficile-associated diarrhea (CDAD), formerly pseudomembranous colitis, has been reported with almost all antibacterial drugs and may range from mild diarrhea to fatal colitis. The most common culprits include clindamycin and lincomycin. Antibacterial therapy alters the normal flora of the colon, leading to overgrowth of C difficile, whose toxins A and B contribute to CDAD development. Morbidity and mortality are increased with hypertoxin-producing strains of C difficile; these infections can be resistant to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea after antibacterial use. Since CDAD has been reported to occur more than 2 months after antibacterial use, careful medical history is necessary. Therapy with broad-spectrum antibacterials and other agents with significant antibacterial activity should be administered cautiously in patients with history of gastrointestinal disease, particularly colitis; pseudomembranous colitis (generally characterized by severe, persistent diarrhea and severe abdominal cramps, and sometimes associated with the passage of blood and mucus), if it occurs, may be more severe in these patients and may be associated with flares in underlying disease activity. Antibacterial drugs not directed against C difficile may need to be stopped if CDAD is suspected or confirmed. Appropriate fluid and electrolyte management, protein supplementation, antibacterial treatment of C difficile, and surgical evaluation should be started as clinically indicated.
31 sources
- "Product Information. Omnipen (ampicillin)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Ceftin (cefuroxime)." Glaxo Wellcome (2002):
- "Product Information. Zinacef (cefuroxime)." Glaxo Wellcome (2002):
- "Product Information. Cleocin (clindamycin)." Pharmacia and Upjohn (2002):
- "Product Information. Macrobid (nitrofurantoin)." Procter and Gamble Pharmaceuticals (2002):
- "Product Information. Macrodantin (nitrofurantoin)." Procter and Gamble Pharmaceuticals (2002):
- "Product Information. Amoxil (amoxicillin)." SmithKline Beecham (2001):
- "Product Information. Merrem (meropenem)." Astra-Zeneca Pharmaceuticals (2001):
Show all 31 sourcesShow fewer sources
- "Product Information. Coly-Mycin M Parenteral (colistimethate)." Parke-Davis (2001):
- "Product Information. Lincocin (lincomycin)." Pharmacia and Upjohn (2001):
- "Product Information. Cubicin (daptomycin)." Cubist Pharmaceuticals Inc (2003):
- "Product Information. Xifaxan (rifaximin)." Salix Pharmaceuticals (2004):
- "Product Information. Doribax (doripenem)." Ortho McNeil Pharmaceutical (2007):
- "Product Information. Penicillin G Procaine (procaine penicillin)." Monarch Pharmaceuticals Inc (2009):
- "Product Information. Vibativ (telavancin)." Theravance Inc (2009):
- "Product Information. Teflaro (ceftaroline)." Forest Pharmaceuticals (2010):
- "Product Information. Penicillin G Sodium (penicillin G sodium)." Sandoz Inc (2022):
- "Product Information. Dalvance (dalbavancin)." Durata Therapeutics, Inc. (2014):
- "Product Information. Orbactiv (oritavancin)." The Medicines Company (2014):
- "Product Information. Bicillin C-R (benzathine penicillin-procaine penicillin)." A-S Medication Solutions (2017):
- "Product Information. Baxdela (delafloxacin)." Melinta Therapeutics, Inc. (2017):
- "Product Information. Polymyxin B Sulfate (polymyxin B sulfate)." AuroMedics Pharma LLC (2022):
- "Product Information. Zemdri (plazomicin)." Achaogen (2018):
- "Product Information. Seysara (sarecycline)." Allergan Inc (2018):
- "Product Information. Nuzyra (omadacycline)." Paratek Pharmaceuticals, Inc. (2018):
- "Product Information. Aemcolo (rifamycin)." Aries Pharmaceuticals, Inc. (2018):
- "Product Information. Fetroja (cefiderocol)." Shionogi USA Inc (2019):
- "Product Information. Biaxin (clarithromycin)." AbbVie US LLC (2019):
- "Product Information. Zithromax (azithromycin)." Pfizer U.S. Pharmaceuticals Group (2021):
- "Product Information. E.E.S.-400 Filmtab (erythromycin)." Arbor Pharmaceuticals (2018):
- "Product Information. Priftin (rifapentine)." sanofi-aventis (2020):
Premature Birth
MajorParenteral medications formulated in multidose vials often contain benzyl alcohol as a preservative. Their use is considered by drug manufacturers to be contraindicated in neonates, particularly premature infants and infants of low birth weight. When used in bacteriostatic saline intravascular flush and endotracheal tube lavage solutions, benzyl alcohol has been associated with fatalities and severe respiratory and metabolic complications in low-birth-weight premature infants. Thus, single-dose formulations should always be used in infants whenever possible. However, many experts feel that, in the absence of benzyl alcohol-free equivalents, the amount of the preservative present in these formulations should not necessarily preclude their use if they are clearly indicated. The American Academy of Pediatrics considers benzyl alcohol in low doses (such as when used as a preservative in some medications) to be safe for newborns. However, the administration of high dosages of these medications must take into account the total amount of benzyl alcohol administered. The level at which toxicity may occur is unknown.
6 sources
- "Product Information. Fragmin (dalteparin)." Pharmacia and Upjohn (2001):
- "Product Information. Mesnex (mesna)." Bristol-Myers Squibb (2001):
- "Product Information. Mivacron (mivacurium)." Glaxo Wellcome (2001):
- "Product Information. Nuromax (doxacurium)." Glaxo Wellcome (2001):
- "Product Information. Tracrium (atracurium)." Glaxo Wellcome (2001):
- ""Inactive" ingredients in pharmaceutical products: update (subject review). American Academy of Pediatrics Committee on Drugs. Available from: URL: http://www.aap.org/policy/re9706.html." Pediatrics 99 (1997): 268-78
Kidney Diseases
ModerateClindamycin is eliminated by the kidney to a limited extent. Therapy with clindamycin should be administered cautiously in patients with severely impaired renal function. Dosage adjustments are probably not necessary. However, serum clindamycin concentrations should be monitored during high-dose therapy, and periodic renal function tests should be performed during prolonged therapy.
3 sources
- Eastwood JB, Gower PE "A study of the pharmacokinetics of clindamycin in normal subjects and patients with chronic renal failure." Postgrad Med J 50 (1974): 710-2
- Peddie BA, Dann E, Bailey RR "The effect of impairment of renal function and dialysis on the serum and urine levels of clindamycin." Aust N Z J Med 5 (1975): 198-202
- "Product Information. Cleocin (clindamycin)." Pharmacia and Upjohn (2002):
Liver Diseases
ModerateClindamycin is primarily metabolized by the liver. The serum concentration of clindamycin may be increased and the half-life prolonged in patients with severely impaired hepatic function. In addition, jaundice and liver enzyme abnormalities may occur during use of the drug. Therapy with clindamycin should be administered cautiously in patients with liver disease. Dosage adjustments may not be necessary when administered every 8 hours. However, serum concentrations should be monitored during high-dose therapy, and periodic liver function tests should be performed during prolonged therapy.
4 sources
- Avant GR, Schenker S, Alford RH "The effect of cirrhosis on the disposition and elimination of clindamycin." Dig Dis 20 (1975): 223-30
- Hinthorn DR, Baker LH, Romig DA, et al. "Use of clindamycin in patients with liver disease." Antimicrob Agents Chemother 9 (1976): 498-501
- Eng RH, Gorski S, Person A, et al. "Clindamycin elimination in patients with liver disease." J Antimicrob Chemother 8 (1981): 277-81
- "Product Information. Cleocin (clindamycin)." Pharmacia and Upjohn (2002):