(Drug Name) (Drug Form) (Drug Strength)
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Iprivask: Lyophilisate for solution for injection (15mg)

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What is this Medicine?

DESIRUDIN is an anticoagulant. It is used to help prevent blood clots in patients having hip replacement surgery.

In-Depth Information
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Iprivask 15mg Powder for Injection Kit

NDC: 512920111
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Deep Venous Thrombosis (DVT) Prophylaxis

Sometimes used for but not FDA approved for the following conditions:
Acute Myocardial Infarction, Percutaneous Transluminal Coronary Angioplasty (PTCA), Unstable Angina

Storage Information
Protect from light
Reconstituted product may be stored at 77 degrees F, excursions permitted to 59-86 degrees F, then discarded after 24 hours
Store unreconstituted product at 77 degrees F; excursions permitted to 59-86 degrees F
Iprivask 15mg Powder for Injection Kit

Reported Side Effects for Iprivask 15mg Powder for Injection Kit

Upset Stomach Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Blood Clot Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Skin Irritation Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Bleeding Within The Eye Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Decreased Healing Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Vomiting Of Blood Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Lightheadedness Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Antibody Formation Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Anaphylactoid Reactions Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Vomiting Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Bleeding In The Abdomen Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Bleeding In The Brain Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Blood In The Urine Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Intestinal Bleeding Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Low Blood Pressure Incidence:
<1.0%*
Severity: MODERATE
Onset: RAPID
Fever Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Nose Bleed Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Swelling Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Irritated Blood Vessels Incidence:
2.0%*
Severity: MODERATE
Onset: RAPID
Anemia Incidence:
3.0%*
Severity: MODERATE
Onset: DELAYED
Injection Site Reaction Incidence:
4.0%*
Severity: MILD
Onset: RAPID
Bruise Incidence:
6.0%*
Severity: MODERATE
Onset: EARLY
Bleeding Incidence:
30.0%*
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

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


Learning More About
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