Lovenox Solution For Injection 100Mg Drug Medication Dosage Information
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Lovenox: Solution for injection (100mg)

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Lovenox 100mg/ml Soln for Inj
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Lovenox 300mg/3ml Sol for Inj

CVS Pharmacy Patient Statistics for Lovenox: Solution for injection(100mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
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Lovenox 100mg/ml Solution for Injection

NDC: 000750623
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Acute Myocardial Infarction, Deep Venous Thrombosis (DVT), Unstable Angina, Coronary Artery Thrombosis Prophylaxis, Pulmonary Embolism

Sometimes used for but not FDA approved for the following conditions:
Percutaneous Coronary Intervention (PCI), Cerebral Thromboembolism, Arterial Thromboembolism Prophylaxis, Deep Venous Thrombosis (DVT) Prophylaxis, Antiphospholipid Antibody Syndrome, Pulmonary Embolism Prophylaxis, Obesity, Thrombosis Prophylaxis

Storage Information
Store at 77 degrees F; excursions permitted to 59-86 degrees F
Lovenox 100mg/ml Solution for Injection

Reported Side Effects for Lovenox 100mg/ml Solution for Injection

Blood In The Urine Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Bruise Incidence:
<3.0%*
Severity: MILD
Onset: DELAYED
Bruise Incidence:
<9.0%*
Severity: MODERATE
Onset: EARLY
Anemia Incidence:
<16.0%*
Severity: MODERATE
Onset: DELAYED
Bleeding Incidence:
<13.0%*
Severity: SEVERE
Onset: EARLY
Low Platelet Count Incidence:
0.1-1.5%*
Severity: MODERATE
Onset: DELAYED
Fluid In Lungs Incidence:
0.7%*
Severity: SEVERE
Onset: EARLY
Irregular Heart Beat Incidence:
0.7%*
Severity: SEVERE
Onset: EARLY
Bleeding In The Brain Incidence:
0.8%*
Severity: SEVERE
Onset: DELAYED
Heart Failure Incidence:
1.0%*
Severity: SEVERE
Onset: DELAYED
Swelling Incidence:
2.0%*
Severity: MODERATE
Onset: DELAYED
Loose Stools Incidence:
2.2%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
2.5-3.0%*
Severity: MILD
Onset: EARLY
Fluid Retention Incidence:
3.0-6.0%*
Severity: MODERATE
Onset: DELAYED
Shortness Of Breath Incidence:
3.3%*
Severity: MODERATE
Onset: EARLY
Fever Incidence:
5.0-8.0%*
Severity: MILD
Onset: EARLY
Elevated Hepatic Enzymes Incidence:
5.9-6.1%*
Severity: MODERATE
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

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


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