Drug lookup
Drug reference

Dalbavancin

Lipoglycopeptide antibiotic (long-acting) · Antibiotic

Also known as Xydalba, Dalbavancin hydrochloride

START
1500 mg IV single dose over 30 min
TYPICAL MAX
1500 mg single (or 1000 + 500 mg 1 week apart)
STOP IF
Anaphylaxis or significant hepatotoxicity
WATCH
Infusion rate (reaction), LFTs, CDI symptoms, renal function
CDSCO approvedSchedule HATC J01XA04
Dose laddermg/d
500wk-2 dose1kwk-1 dose1.5ksingle max
Renal dose adjustmenteGFR mL/min/1.73m²
FULLStandard dosing30REDUCEReduce dose if not on haemodialysis90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
6minONSET30minPEAK2.1w2wDURATION
ONSET
6min · infusion start
PEAK
30min · end infusion
2.1w · t½ ~14 d
DURATION
2w · single-dose cover
EXCRETION
Renal ~33% unchanged; faecal remainder
route + CYP
INTERACTIONS
none in our sources
PREGNANCY
Limited data; use only if clearly needed.
FDA category + note

Mechanism

Binds the D-alanyl-D-alanine terminus of peptidoglycan precursors, inhibiting bacterial cell-wall transglycosylation/transpeptidation; bactericidal against Gram-positive organisms including MRSA, with a very long half-life.

Indications

Acute bacterial skin and skin-structure infections (Gram-positive, including MRSA)

Dosing

Adult
1500 mg IV single dose over 30 min, OR 1000 mg IV then 500 mg IV one week later.
Pediatric
Weight-based single dose (approved in children; specialist).
Renal adjustment
CrCl <30 and not on haemodialysis: reduce (e.g., 1125 mg single, or 750 mg then 375 mg). No adjustment if on HD.
Hepatic adjustment
Mild: no adjustment; moderate–severe: caution (limited data).
Geriatric
No adjustment beyond renal function.
Max dose
1500 mg single dose (or 1000 + 500 mg one week apart)

Pharmacokinetics

Onset
Bactericidal levels from end of infusion
Peak effect
End of infusion
Duration
Therapeutic levels for ~1–2 weeks (single dose)
Half-life
~346 h (~14 days)
Bioavailability
IV 100%
Protein binding
~93%
Metabolism
Minimal (hydroxy-dalbavancin minor)
Excretion
Renal (~33% unchanged) and faecal

Contraindications

  • Hypersensitivity to dalbavancin/glycopeptides
  • Caution: vancomycin hypersensitivity (possible cross-reaction)

Side effects

Common
NauseaHeadacheDiarrhoeaRashTransient ALT elevation
Serious
  • Anaphylaxis/serious hypersensitivity
  • Infusion-related reaction ('red man'-type with rapid infusion)
  • Hepatotoxicity
  • Clostridioides difficile colitis

Pregnancy & lactation

Pregnancy

Limited data; use only if clearly needed.

Lactation

Limited data; caution.

Drug interactions

Live Bacterial Vaccines
Moderate
Database

Antibacterial inactivation

Separate appropriately

Source: Kimi deep-research + Cla

Vancomycin
Moderate
Database

Glycopeptide cross-reactivity

Caution if prior vancomycin reaction

Source: Kimi deep-research + Cla

Hepatotoxic Drugs
Mild
Database

Additive hepatic effect

Monitor LFTs

Source: Kimi deep-research + Cla

Nephrotoxic Drugs
Mild
Database

Partial renal elimination

Monitor renal function

Source: Kimi deep-research + Cla

Other Qt
Mild
Database

No specific PK interaction

Standard antibiotic monitoring

Source: Kimi deep-research + Cla

6 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Ask House about Dalbavancin

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: Goodman & Gilman 14e, Harrison 22e, Katzung, BNF·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20