Isentress Granules For Oral Suspension 100Mg Drug Medication Dosage Information
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Isentress: Granules for oral suspension (100mg)

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What is this Medicine?

RALTEGRAVIR (ral TEG ra veer) is an antiretroviral medicine. It is used with other medicines to treat HIV. This medicine is not a cure for HIV. It will not stop the spread of HIV to others.

In-Depth Information

Isentress 100mg Granules for Suspension

NDC: 000063603
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Human Immunodeficiency Virus (HIV) Infection

Storage Information
Store in original package until time of use
Discard reconstituted product if not used within 30 minutes
Store between 68 to 77 degrees F, excursions permitted 59 to 86 degrees F
Isentress 100mg Granules for Suspension

Reported Side Effects for Isentress 100mg Granules for Suspension

High Amylase Levels Incidence:
<4.0%*
Severity: MODERATE
Onset: DELAYED
Weakness Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Vomiting Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
Thoughts Of Suicide Incidence:
<2.0%*
Severity: SEVERE
Onset: DELAYED
Infection Incidence:
<2.0%*
Severity: MILD
Onset: DELAYED
Liver Infection Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Stomach Pain Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
Low Platelet Count Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Kidney Stones Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Kidney Failure Incidence:
<2.0%*
Severity: SEVERE
Onset: DELAYED
Inflamed Stomach Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
Depression Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Anemia Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Low White Blood Cells Incidence:
1.0-4.0%*
Severity: MODERATE
Onset: DELAYED
Elevated Hepatic Enzymes Incidence:
2.0-34.0%*
Severity: MODERATE
Onset: DELAYED
Lightheadedness Incidence:
2.0%*
Severity: MILD
Onset: EARLY
Increased Blood Sugar Incidence:
2.0-10.0%*
Severity: MODERATE
Onset: DELAYED
Headache Incidence:
2.0-4.0%*
Severity: MILD
Onset: EARLY
Tired Incidence:
2.0%*
Severity: MILD
Onset: EARLY
High Bilirubin Level Incidence:
3.0-17.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
3.0%*
Severity: MILD
Onset: EARLY
Inability To Sleep Incidence:
4.0%*
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

Avoid - This drug is known to cause harm to infants when taken by nursing mothers.


Learning More About
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