Dalvance Lyophilisate For Solution For Injection 500Mg Drug Medication Dosage Information
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DALVANCE: Lyophilisate for solution for injection (500mg)

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What is this Medicine?

DALBAVANCIN (DAL ba van sin) is an antibiotic. It is used to treat certain kinds of bacterial infections. It will not work for colds, flu, or other viral infections.

In-Depth Information

Dalvance 500mg Powder for Injection

NDC: 579700100
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Cellulitis, Skin And Skin Structure Infections

Storage Information
Discard product if it contains particulate matter, is cloudy, or discolored
Discard unused portion. Do not store for later use.
Reconstituted product may be stored in refrigerator (36 to 46 degrees F) or at room temperature (up to 77 degrees F)
Store unreconstituted product at 77 degrees F; excursions permitted to 59-86 degrees F
Dalvance 500mg Powder for Injection

Reported Side Effects for Dalvance 500mg Powder for Injection

Irritated Blood Vessels Incidence:
<2.0%*
Severity: MODERATE
Onset: RAPID
Red Spotted Rash Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Melena Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Bruise Incidence:
<2.0%*
Severity: MODERATE
Onset: EARLY
Flushing Incidence:
<2.0%*
Severity: MILD
Onset: RAPID
Eosinophilia Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Elevated Hepatic Enzymes Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Lightheadedness Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
Breathing Difficulties Incidence:
<2.0%*
Severity: SEVERE
Onset: RAPID
Anaphylactoid Reactions Incidence:
<2.0%*
Severity: SEVERE
Onset: RAPID
Infusion-related Reactions Incidence:
<2.0%*
Severity: MODERATE
Onset: RAPID
Skin Rash Incidence:
<2.7%*
Severity: MILD
Onset: EARLY
Low White Blood Cell Counts Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Intestinal Bleeding Incidence:
<2.0%*
Severity: SEVERE
Onset: DELAYED
Stomach Pain Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
Hives Incidence:
<2.0%*
Severity: MILD
Onset: RAPID
High Platelet Count Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Low Platelet Count Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Pseudomembranous Colitis Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Itching Incidence:
<2.1%*
Severity: MILD
Onset: RAPID
Low White Blood Cells Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Low Blood Sugar Incidence:
<2.0%*
Severity: MODERATE
Onset: EARLY
Yeast Infection Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Anemia Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
2.0-5.5%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
2.8%*
Severity: MILD
Onset: EARLY
Loose Stools Incidence:
3.4-4.4%*
Severity: MILD
Onset: EARLY
Headache Incidence:
3.8-4.7%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


Learning More About
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