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Clindamicina

Clindamycin

Clindamycin hydrochloride, Clindamycin palmitate hydrochloride, Clindamycin phosphate

Antibiótico lincosamidaPOIMIVSCtopicalPerrosGatosHuronesAvesReptiles

También conocido como: Antirobe · Cleocin · Clintabs · Clinsol · Clinacin · Clindacyl · Clindaseptin · Mycinor · Zodon · chlorodeoxylincomycin hydrochloride · (7S)-chloro-7-deoxy-lincomycin hydrochloride · clindamycini hydrochloridum · U-28508 · U-25179E · Clindamycine · Clindamicina

Revisado por el equipo veterinario de VetSheetActualizado 5 abr 2026Referencia veterinaria basada en la evidencia

Antibiótico de importancia alta según la OMSse recomienda el uso responsable
5.5-33 mg/kgPO· q12h· Up to 28 days
🐕

Las dosis son una referencia clínica para profesionales veterinarios autorizados. Confirme siempre con el prospecto actual y cada paciente individual.

Dosis por especie

🌎 NA — North America🌍 EU — Europe

Perros

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Infected wounds, abscesses and dental infections5.5-33 mg/kgPOq12hUp to 28 days🌎 NA
Osteomyelitis11-33 mg/kgPOq12hUp to 28 days🌎 NA
Staphylococcal pyoderma11 mg/kgPOonce daily7-28 days🌎 NA
Wounds, abscesses, dental infections, stomatitis5-11 mg/kgPOq12h7-28 days🌎 NA
Osteomyelitis11 mg/kgPOq12h28 days🌎 NA
Systemic bacteremia3-10 mg/kgIV, IM, SC, POq8has long as needed🌎 NA
Susceptible bacterial infections5-11 mg/kgIM, SC, POq12h🌎 NA
Sepsis11 mg/kgIVq12h🌎 NA
Recurrent superficial pyodermas11 mg/kgPOonce daily to twice a day🌎 NA
Actinomycosis5 mg/kgSCq12h🌎 NA
Susceptible hepatobiliary infections10-16 mg/kg SC once daily or 5-10 mg/kg PO q12hSC, POonce daily or q12h🌎 NA
Anaerobic infections5-10 mg/kgPO, IVq12h🌎 NA
Intra-abdominal sepsis5-11 mg/kgIV, SC, POq8-12h5-7 days🌎 NA
Pancreatitis5-11 mg/kgIV, SC, POq8-12h3-5 days🌎 NA
Susceptible respiratory infections10 mg/kgPO, SCq12h🌎 NA
Surgical prophylaxis for gram-positive aerobes and anaerobic coverage5-11 mg/kgPOonce16-60 minutes preoperatively🌎 NA
Toxoplasmosis12.5 mg/kgPO, IMq12h28 days🌎 NA
Neospora10 mg/kgPOq12h4 weeks🌎 NA
Hepatozoon canis10 mg/kgPOq8h2-4 weeks🌎 NA
Babesia spp.12.5 mg/kgPOq12h2 weeks🌎 NA
Babesia infections (if specific antibabesial drugs are not available)25 mg/kgPOq12h7-21 days🌎 NA
Hepatozoon americanum infections10 mg/kgPOq8h14 days🌎 NA
Susceptible infections5.5 mg/kgPOq12h🌍 EU
Severe infections11 mg/kgPOq12h🌍 EU
Toxoplasmosis/neosporosis25 mg/kgPOdaily in divided doses🌍 EU
  • Infected wounds, abscesses and dental infections: If no response after 3-4 days, discontinue.
  • Osteomyelitis: If no response after 3-4 days, discontinue.
  • Susceptible bacterial infections: Avoid or reduce dose in patients with severe liver failure
  • Recurrent superficial pyodermas: Resistance can develop quickly
  • Susceptible hepatobiliary infections: In patients with liver function impairment: 5 mg/kg PO q12h or SC q24h
  • Intra-abdominal sepsis: Combined with gentamicin or a parenteral 3rd generation cephalosporin or enrofloxacin
  • Neospora: Used concurrently with trimethoprim/sulfa (15 mg/kg PO q12h for 4 weeks)
  • Hepatozoon canis: Use concurrently with pyrimethamine and trimethoprim/sulfa
  • Hepatozoon americanum infections: Use concurrently with trimethoprim/sulfa and pyrimethamine, follow with decoquinate
  • Susceptible infections: Alternatively, 11 mg/kg q24h

Gatos

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Susceptible bacterial infections5-10 mg/kgPOq12h🌎 NA
Infected wounds, abscesses and dental infections11-33 mg/kgPOonce a day (q24h)Maximum 14 days🌎 NA
Sepsis11 mg/kgIVq12h🌎 NA
Anaerobic infections5-10 mg/kgPO, IVq12h🌎 NA
Intra-abdominal sepsis5-11 mg/kgIV, SC, POq8-12h5-7 days🌎 NA
Pancreatitis5-11 mg/kgIV, SC, POq8-12h3-5 days🌎 NA
Susceptible respiratory infections10-15 mg/kgPO, SCq12h🌎 NA
Surgical prophylaxis for gram-positive aerobes and anaerobic coverage5-11 mg/kgPOonce16-60 minutes preoperatively🌎 NA
Toxoplasmosis (to decrease zoonotic risk by reducing shedding period)25-50 mg/kgPOdaily🌎 NA
Clinical toxoplasmosis10 mg/kgPOq12hat least 28 days🌎 NA
Enteroepithelial toxoplasmosis8-16 mg/kgPO, SCq8h14-28 days🌎 NA
Systemic toxoplasmosis12.5-25 mg/kgPO, SCq12h14-28 days🌎 NA
  • Infected wounds, abscesses and dental infections: Do not treat acute infections for more than 3-4 days if no clinical response is seen.
  • Intra-abdominal sepsis: Combined with gentamicin or a parenteral 3rd generation cephalosporin or enrofloxacin
  • Clinical toxoplasmosis: Institute supportive care as needed.

Hurones

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Susceptible infections5-10 mg/kgPOtwice daily🌎 NA

Aves

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Susceptible infections25 mg/kgPOq8h🌎 NA
Mild spore-forming enteric bacterial infections50 mg/kgPOq12h5-10 days🌎 NA

Reptiles

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Susceptible infections (anaerobes)5 mg/kgPOonce daily🌎 NA
Respiratory infections (anaerobes, mycoplasma)5 mg/kgPOonce daily14 days🌎 NA

Las dosis son una referencia clínica para profesionales veterinarios autorizados. Confirme siempre con el prospecto actual y cada paciente individual.

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Resumen

La clindamicina es un antibiótico lincosamida de amplio espectro ampliamente utilizado en medicina veterinaria. Es altamente eficaz contra muchas bacterias anaerobias, cocos aerobios grampositivos (como Staphylococcus y Streptococcus) y ciertos protozoos, incluyendo Toxoplasma, Neospora y Babesia.

​Perlas clínicas:​

  • ​Excelente penetración tisular:​ La clindamicina alcanza altas concentraciones en hueso, líquido sinovial, abscesos y glóbulos blancos, lo que la convierte en una opción de primera línea para osteomielitis, infecciones dentales y piodermia profunda.
  • ​Toxoplasmosis:​ Es un tratamiento primario para la toxoplasmosis clínica en gatos y perros.
  • ​Toxicidad en herbívoros:​ Está estrictamente contraindicada en fermentadores de intestino posterior (caballos, conejos, roedores) y rumiantes debido al riesgo de enterocolitis clostridial mortal.
  • ​Riesgo de estenosis esofágica:​ En gatos, administrar cápsulas o tabletas en seco puede causar esofagitis grave y estenosis. Siempre acompañe las dosis sólidas orales con un bolo de agua o comida.

Mecanismo de acción

Clindamycin acts by binding to the 50S ribosomal subunit of susceptible bacteria.

  • ​Mechanism:​ It inhibits peptide bond formation (transpeptidation) → blocks bacterial protein synthesis.
  • ​Effect:​ It can be either bacteriostatic or bactericidal, depending on the drug concentration at the infection site and the specific susceptibility of the organism.
  • ​Resistance:​ Complete cross-resistance occurs between clindamycin and lincomycin, and partial cross-resistance occurs with macrolides (like erythromycin) due to overlapping ribosomal binding sites.

Seguridad y advertencias

Contraindicaciones

  • Horses
  • Rabbits
  • Hamsters
  • Chinchillas
  • Guinea pigs
  • Ruminants
  • Patients hypersensitive to lincosamides
  • Neonatal small animals (generally avoided)
  • Known hypersensitivity to lincosamides

Efectos adversos

  • Gastroenteritis (emesis, loose stools, bloody diarrhea)
  • Esophageal injuries (esophagitis, strictures) in cats if dry-pilled
  • Hypersalivation or lip smacking in cats after oral administration
  • Pain at IM injection site
  • Mild, clinically insignificant increases in liver enzymes (AST, ALT, ALP)
  • Colitis
  • Vomiting
  • Diarrhoea
  • Oesophagitis (especially in cats)
  • Oesophageal stricture (especially in cats)

Precauciones

​Esophageal Injury Warning:​ Clindamycin has been implicated in causing esophagitis and esophageal strictures in small animals (especially cats). ​Avoid dry 'pilling'​; always administer with food or a water bolus.

  • ​Hepatic/Renal Impairment:​ Patients with very severe renal and/or hepatic disease should receive the drug with caution. Consider dosage reduction and monitor serum clindamycin levels during high-dose therapy.
  • ​Species Restrictions:​ Fatal gastrointestinal effects can occur in horses, ruminants, and small herbivores (rabbits, rodents). Do not use in these species.

Interacciones farmacológicas

Cyclosporine

Clindamycin may reduce cyclosporine levels

Erythromycin

In vitro antagonism when used with clindamycin; concomitant use should probably be avoided

Neuromuscular blocking agents (e.g., pancuronium)

Clindamycin possesses intrinsic neuromuscular blocking activity and should be used cautiously with other neuromuscular blocking agents

Non-depolarizing muscle relaxants (e.g., tubocurarine)Major

May enhance the neuromuscular blocking effect

NeostigmineModerate

May antagonize the effects of neostigmine

PyridostigmineModerate

May antagonize the effects of pyridostigmine

Macrolides (e.g., erythromycin)Major

Antagonistic antimicrobial effects due to competing binding sites

ChloramphenicolMajor

Antagonistic antimicrobial effects due to competing binding sites

Other lincosamidesMajor

Antagonistic antimicrobial effects

Tubocurarine (and other non-depolarizing muscle relaxants)Moderate

May enhance the neuromuscular blocking effect

LincomycinMajor

Complete cross-resistance and antagonistic effect

Monitorización

  • Clinical efficacy
  • Adverse effects; particularly severe diarrhea
  • Periodic liver and kidney function tests and blood counts if therapy persists for more than 30 days
  • Gastrointestinal signs (vomiting, diarrhoea)
  • Hepatic and renal function in patients with pre-existing impairment

Farmacocinética

Vida media

Perros2-5 hours (PO), 10-13 hours (SC)

Absorción

Rapidly absorbed from the gut. In dogs, oral bioavailability is about 73%. Food decreases the rate of absorption, but not the extent. Peak serum levels are attained about 45-60 minutes after oral dosing.

Distribución

Distributes well into most tissues. Therapeutic levels are achieved in bone, synovial fluid, bile, pleural fluid, peritoneal fluid, skin, heart muscle, abscesses, scar tissue, and white blood cells. CNS levels may reach 40% of serum levels if meninges are inflamed. About 93% bound to plasma proteins. Crosses the placenta and distributes into milk.

Metabolismo

Partially metabolized in the liver to both active and inactive metabolites.

Eliminación

Unchanged drug and metabolites are excreted in the urine, feces, and bile. Half-lives can be prolonged in patients with severe renal or hepatic dysfunction.

Sobredosis

There is little information available regarding overdoses of this drug.

  • In dogs, oral doses of up to 300 mg/kg/day for up to one year did not result in toxicity.
  • Dogs receiving 600 mg/kg/day developed anorexia, vomiting, and weight loss.

Productos disponibles

Formulaciones

  • Oral capsules
  • Oral tablets
  • Oral solution/drops
  • Granules for oral solution
  • Injection (solution concentrate)
  • Suppositories
  • Topical and vaginal preparations
  • 25 mg capsule/tablet
  • 75 mg capsule/tablet
  • 88 mg capsule/tablet
  • 150 mg capsule/tablet
  • 264 mg capsule/tablet
  • 300 mg capsule/tablet
  • 25 mg/ml oral solution

Veterinario

  • Clindamycin (as HCl) Oral Capsules: 25 mg, 75 mg, 150 mg, 300 mg (Antirobe, generics)
  • Clindamycin (as HCl) Oral Tablets: 25 mg, 75 mg, 150 mg (Clintabs)
  • Clindamycin (as HCl) Oral Solution: 25 mg/mL (Antirobe Aquadrops, Clinsol, generics)
  • Clinacin
  • Clindacyl
  • Clindaseptin
  • Mycinor
  • Zodon

Etiquetado para humanos

  • Clindamycin (as HCl) Oral Capsules: 75 mg, 150 mg, 300 mg (Cleocin, generics)
  • Clindamycin (as palmitate HCl) Granules for Oral Solution: 75 mg/5 mL (Cleocin Pediatric)
  • Clindamycin (as Phosphate) Solution Concentrate for Injection: 150 mg/mL (Cleocin Phosphate)
  • Clindamycin (as Phosphate) Injection: 300 mg, 600 mg, 900 mg in Galaxy containers (Cleocin Phosphate IV)
  • Clindamycin Phosphate Suppositories: 100 mg (Cleocin)

Estado regulador

European Union✓ AprobadoMedicamento de prescripciónEMA
🐕 Dogs🐈 Cats

POM-V

United Kingdom✓ AprobadoMedicamento de prescripciónVMD
🐕 Dogs🐈 Cats

POM-V

Sin datos reguladores para: 🇺🇸 US · 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

Almacenamiento y estabilidad

Capsules and palmitate powder for oral solution should be stored at room temperature (15-30°C). After reconstitution, the human palmitate oral solution should NOT be refrigerated (thickening may occur) and is stable for 2 weeks at room temp. Veterinary oral solution has an extended shelf life at room temp. Phosphate injection should be stored at room temp; if refrigerated, crystals may form but will resolubilize upon warming.

Información para el cliente

​Nota importante sobre la administración:​ Si utiliza tabletas o cápsulas orales, especialmente en gatos, siempre acompañe el medicamento con al menos 6 mL (un poco más de una cucharadita) de líquido o escóndalo en una pequeña bola de comida húmeda. Administrar una pastilla en seco puede causar que el medicamento se pegue en el esófago, provocando úlceras graves y estenosis.

  • ​Vigile los problemas gastrointestinales:​ Informe a su veterinario inmediatamente si observa cualquier incidencia de diarrea grave, prolongada o con sangre.
  • ​Complete el tratamiento:​ Administre el medicamento exactamente como se le recetó durante todo el tiempo indicado, incluso si su mascota parece sentirse mejor, para prevenir infecciones resistentes.

La referencia de medicamentos de VetSheet está destinada a profesionales veterinarios autorizados como ayuda para la toma de decisiones clínicas, no como sustituto del criterio profesional ni del prospecto actual del fabricante.