Apidra Solostar Solution For Injection 100U Drug Medication Dosage Information
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Apidra SoloStar: Solution for injection (100U)

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Apidra SoloStar 100unit/ml Pen

What is this Medicine?

INSULIN GLULISINE (IN su lin; GLOO lis een) is a human-made form of insulin. This medicine lowers the amount of sugar in your blood. It is a fast acting insulin that starts working faster than regular insulin. It will not effect your blood sugar as long as regular insulin.

Similar Brand Name Drugs : Apidra: Solution for injection (100U)
CVS Pharmacy Patient Statistics for Apidra SoloStar: Solution for injection(100U)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Apidra SoloStar 100units/ml Pre-Filled Pen Solution for Injection

NDC: 000882502
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus

Storage Information
Protect from light
Discard product if it contains particulate matter, is cloudy, or discolored
Opened container can be stored for up to 28 days at room temperature (below 77 degrees F)
Unrefrigerated product must be used within 28 days or be discarded
Store unopened containers in refrigerator (36 to 46 degrees F)
Do not freeze
Discard if product has been frozen
Avoid direct heat and sunlight
Apidra SoloStar 100units/ml Pre-Filled Pen Solution for Injection

Reported Side Effects for Apidra SoloStar 100units/ml Pre-Filled Pen Solution for Injection

Skin Rash Incidence:
<4.3%*
Severity: MILD
Onset: EARLY
Severe Low Blood Sugar Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Anaphylactoid Reactions Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
High Blood Pressure Incidence:
3.9%*
Severity: MODERATE
Onset: EARLY
Flu Incidence:
4.0-6.2%*
Severity: MILD
Onset: DELAYED
Headache Incidence:
5.0-7.0%*
Severity: MILD
Onset: EARLY
Infection Incidence:
6.6-10.5%*
Severity: MILD
Onset: DELAYED
Fluid Retention Incidence:
7.5%*
Severity: MODERATE
Onset: DELAYED
Sore Throat Incidence:
7.6-10.6%*
Severity: MILD
Onset: DELAYED
Low Blood Sugar Incidence:
>10.0%*
Severity: MODERATE
Onset: EARLY
Infusion-related Reactions Incidence:
10.3%*
Severity: MODERATE
Onset: RAPID
*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

Compatible - This drug is generally safe to take by nursing mothers.


Learning More About
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