Xeomin Lyophilisate For Solution For Injection 100U Drug Medication Dosage Information
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Xeomin: Lyophilisate for solution for injection (100U)

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What is this Medicine?

INCOBOTULINUMTOXINA (IN koh BOT ue LYE num TOX in AY) is a neuro-muscular blocker. This medicine is used to treat eyelid spasms and severe neck muscle spasms. It is also used to treat moderate to severe frown lines on the face.

In-Depth Information

Xeomin 100unit Powder for Injection

NDC: 002591610
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Facial Wrinkles, Cervical Dystonia, Blepharospasm, Spasticity

Storage Information
Store unopened product at room temperature (68 to 77 degree F), in refrigerator (36 to 46 degrees F), or freezer (-4 to 14 degrees F) for up to 36 months
Store reconstituted product in refrigerator (36 to 46 degrees F) and administer within 24 hours
Xeomin 100unit Powder for Injection

Reported Side Effects for Xeomin 100unit Powder for Injection

Weakness Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Back Pain Incidence:
<5.0%*
Severity: MILD
Onset: DELAYED
Swollen Eyelids Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Blurred Vision Incidence:
<12.0%*
Severity: MODERATE
Onset: EARLY
Bruise Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Injection Site Reaction Incidence:
<9.0%*
Severity: MILD
Onset: RAPID
Muscle And/Or Bone Pain Incidence:
<7.0%*
Severity: MILD
Onset: EARLY
Paresis Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Drooping Eyelids Incidence:
<19.0%*
Severity: MILD
Onset: DELAYED
Visual Impairment Incidence:
<12.0%*
Severity: SEVERE
Onset: EARLY
Weakness Incidence:
<11.0%*
Severity: MILD
Onset: EARLY
Joint Pain Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Eye Twitch Incidence:
<0.2%*
Severity: MODERATE
Onset: EARLY
Loose Stools Incidence:
<8.0%*
Severity: MILD
Onset: EARLY
Shortness Of Breath Incidence:
<5.0%*
Severity: MODERATE
Onset: EARLY
Headache Incidence:
<7.1%*
Severity: MILD
Onset: EARLY
Muscle Pain Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
Sore Throat Incidence:
<5.0%*
Severity: MILD
Onset: DELAYED
Dry Eyes Incidence:
<16.0%*
Severity: MILD
Onset: EARLY
Dry Mouth Incidence:
<16.0%*
Severity: MILD
Onset: EARLY
Difficulty Swallowing Incidence:
<18.0%*
Severity: MODERATE
Onset: DELAYED
Infection Incidence:
<20.0%*
Severity: MILD
Onset: DELAYED
Antibody Formation Incidence:
1.1%*
Severity: MODERATE
Onset: DELAYED
Light Sensitivity Incidence:
1.4%*
Severity: MODERATE
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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