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TRULICITY: Solution for injection (0.75mg)

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Trulicity 0.75mg/0.5ml Sol Inj

What is this Medicine?

DULAGLUTIDE (DOO la GLOO tide) is used to improve blood sugar control in adults with type 2 diabetes. This medicine may be used with other oral diabetes medicines.

CVS Pharmacy Patient Statistics for TRULICITY: Solution for injection(0.75mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Trulicity 0.75mg/0.5ml Solution for Injection

NDC: 000021433
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Type 2 Diabetes Mellitus

Storage Information
Refrigerate (between 36 and 46 degrees F)
Protect from light
Discard product if it contains particulate matter, is cloudy, or discolored
Do not use if product has been frozen
Store in carton until time of use
Discard unused portion. Do not store for later use.
Do not freeze
Store at or below 86 degrees F, away from heat sources, for up to 14 days if refrigeration is not available
Trulicity 0.75mg/0.5ml Solution for Injection

Reported Side Effects for Trulicity 0.75mg/0.5ml Solution for Injection

Injection Site Reaction Incidence:
0.5%*
Severity: MILD
Onset: RAPID
Skin Rash Incidence:
0.5%*
Severity: MILD
Onset: EARLY
Swelling Incidence:
0.5%*
Severity: MODERATE
Onset: DELAYED
Skin Redness Incidence:
0.5%*
Severity: MODERATE
Onset: EARLY
Hives Incidence:
0.5%*
Severity: MILD
Onset: RAPID
Belching Incidence:
0.6-1.6%*
Severity: MILD
Onset: EARLY
Gas Incidence:
1.4-3.4%*
Severity: MILD
Onset: EARLY
Antibody Formation Incidence:
1.6%*
Severity: MODERATE
Onset: DELAYED
Heartburn Incidence:
1.7-2.0%*
Severity: MILD
Onset: DELAYED
Heart Block Incidence:
1.7-2.3%*
Severity: SEVERE
Onset: EARLY
PR Prolongation Incidence:
2.5-3.2%*
Severity: MODERATE
Onset: RAPID
Rapid Heart Rate Incidence:
2.8-5.6%*
Severity: MODERATE
Onset: RAPID
Constipation Incidence:
3.7-3.9%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
4.1-5.8%*
Severity: MILD
Onset: EARLY
Tired Incidence:
4.2-5.6%*
Severity: MILD
Onset: EARLY
Decreased Appetite Incidence:
4.9-8.6%*
Severity: MILD
Onset: DELAYED
Vomiting Incidence:
6.0-12.7%*
Severity: MILD
Onset: EARLY
Stomach Pain Incidence:
6.5-9.4%*
Severity: MILD
Onset: EARLY
Loose Stools Incidence:
8.9-12.6%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
12.4-21.1%*
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.
Daily Life Interactions for Trulicity 0.75mg/0.5ml Solution for Injection

Elements of your daily lifestyle may have an effect on the medications you are taking. Drug interactions can result in unwanted side effects, reduce the effectiveness of your medicine or possibly increase the action of a particular medicine.

Moderate Lifestyle Interaction
Alcohol and Trulicity 0.75mg/0.5ml Solution for Injection(Dulaglutide)
Alcohol and Dulaglutide(Dulaglutide)
Ethanol may interfere with the actions of Antidiabetic Agents, including Dulaglutide. Alcoholic beverages can increase the risk of low blood sugar, or can cause increased blood sugar due to the calories in these beverages. Limit alcohol containing medicines and beverages if you are using Dulaglutide. You should also learn how to recognize the signs of low blood sugar.
Minor Lifestyle Interaction
Tobacco and Trulicity 0.75mg/0.5ml Solution for Injection(Dulaglutide)
Tobacco and Dulaglutide(Dulaglutide)
If you use tobacco or are trying to quit tobacco use, you may need to monitor your blood sugar more frequently. Nicotine, a component of tobacco, can increase the blood sugar. Also, if you are trying to quit smoking, as your body adjusts to not smoking, your blood sugar levels may change; the actions of Dulaglutide may be increased and this could lead to low blood sugar. Know the symptoms of low or high blood sugar and report them if they occur. Monitor your blood sugar regularly.
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.


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