Genotropin Miniquick Lyophilisate For Solution For Injection 0.2Mg Drug Medication Dosage Information
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Genotropin MiniQuick: Lyophilisate for solution for injection (0.2mg)

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Genotropin Miniquick 0.2mg Inj

CVS Pharmacy Patient Statistics for Genotropin MiniQuick: Lyophilisate for solution for injection(0.2mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Genotropin Miniquick 0.2mg Powder for Injection

NDC: 000132649
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Prader-Willi Syndrome, SHOX (short Stature Homeobox-containing Gene) Deficiency, Noonan Syndrome, Short Bowel Syndrome, Growth Failure, Growth Hormone Deficiency, Turner Syndrome

Storage Information
Store below 77 degrees F
Discard unused portion. Do not store for later use.
Prior to dispensing, store in refrigerator (36 to 46 degrees F)
Protect from light
Do not freeze
Upon dispensing, product may be stored refrigerated (36 to 46 degrees F), or at or below 77 degrees F for up to 3 months
Reconstituted product may be stored refrigerated in its carton at 36 to 46 degrees F for up to 24 hours if not used immediately
Genotropin Miniquick 0.2mg Powder for Injection

Reported Side Effects for Genotropin Miniquick 0.2mg Powder for Injection

Blood In The Urine Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Inflamed Pancreas Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Convulsions Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
High Triglycerides Incidence:
1.0-5.0%*
Severity: MODERATE
Onset: DELAYED
Wrist Nerve Pain Incidence:
1.0-5.0%*
Severity: MILD
Onset: DELAYED
Paresthesias Incidence:
2.0-17.0%*
Severity: MILD
Onset: DELAYED
Hypoesthesia Incidence:
2.0-15.0%*
Severity: MILD
Onset: DELAYED
Antibody Formation Incidence:
2.0%*
Severity: MODERATE
Onset: DELAYED
Back Pain Incidence:
3.0-11.0%*
Severity: MILD
Onset: DELAYED
Weakness Incidence:
3.0-6.0%*
Severity: MILD
Onset: EARLY
Gynecomastia Incidence:
3.0-8.0%*
Severity: MILD
Onset: DELAYED
Weakness Incidence:
3.0-6.0%*
Severity: MILD
Onset: DELAYED
Swelling Incidence:
3.0-45.0%*
Severity: MODERATE
Onset: DELAYED
Fluid Retention Incidence:
3.0-45.0%*
Severity: MODERATE
Onset: DELAYED
Muscle Pain Incidence:
3.0-30.0%*
Severity: MILD
Onset: EARLY
High Blood Pressure Incidence:
3.0-8.0%*
Severity: MODERATE
Onset: EARLY
Tired Incidence:
4.0-9.0%*
Severity: MILD
Onset: EARLY
Loose Stools Incidence:
5.0%*
Severity: MILD
Onset: EARLY
Inability To Sleep Incidence:
5.0%*
Severity: MILD
Onset: EARLY
Underactive Thyroid Incidence:
5.0-16.0%*
Severity: MODERATE
Onset: DELAYED
Chest Pain Incidence:
5.0%*
Severity: MODERATE
Onset: EARLY
Rhinitis Incidence:
5.0-14.0%*
Severity: MILD
Onset: EARLY
Muscle And/Or Bone Pain Incidence:
5.0-14.0%*
Severity: MILD
Onset: EARLY
Depression Incidence:
5.0%*
Severity: MODERATE
Onset: DELAYED
Acne Incidence:
6.0%*
Severity: MILD
Onset: DELAYED
Anemia Incidence:
6.0%*
Severity: MODERATE
Onset: DELAYED
Rash With Pustules Incidence:
6.0%*
Severity: MILD
Onset: EARLY
Headache Incidence:
6.0-18.0%*
Severity: MILD
Onset: EARLY
Inflamed Stomach Incidence:
6.0%*
Severity: MODERATE
Onset: DELAYED
Cough Incidence:
6.0-9.0%*
Severity: MILD
Onset: DELAYED
Elevated Hepatic Enzymes Incidence:
6.0-13.0%*
Severity: MODERATE
Onset: DELAYED
Stomach Pain Incidence:
7.0%*
Severity: MILD
Onset: EARLY
Diaphoresis Incidence:
8.0%*
Severity: MILD
Onset: EARLY
Increased Blood Fats Incidence:
8.0%*
Severity: MODERATE
Onset: DELAYED
Bruise Incidence:
9.0%*
Severity: MODERATE
Onset: EARLY
Increased Blood Sugar Incidence:
>10.0%*
Severity: MODERATE
Onset: DELAYED
Joint Pain Incidence:
11.0-37.0%*
Severity: MILD
Onset: DELAYED
Eosinophilia Incidence:
12.0%*
Severity: MODERATE
Onset: DELAYED
Fever Incidence:
16.0%*
Severity: MILD
Onset: EARLY
Infection Incidence:
32.0%*
Severity: MILD
Onset: DELAYED
*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 B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Second Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Third Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Lactation

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


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