Tinzaparin

Tinzaparin
Black Box Warning
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alejandro Lemor, M.D. [2]

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Black Box Warning

SPINAL/EPIDURAL HEMATOMAS See full prescribing information for complete Boxed Warning. Spinal/Epidural Hematomas: Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include: Use of indwelling epidural catheters Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants. A history of traumatic or repeated epidural or spinal punctures A history of spinal deformity or spinal surgery Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary. Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis

Overview

Tinzaparin is a low molecular weight heparin that is FDA approved for the treatment of acute symptomatic deep vein thrombosis with or without pulmonary embolism. There is a Black Box Warning for this drug as shown here. Common adverse reactions include bleeding, erythema, increase liver function tests, neurologic pain.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

Deep Venous Thrombosis

• Dosage Information

• 175 anti-Xa IU/kg SC once daily for at least 6 days
• Warfarin therapy should be initiated within 1-3 days of tinzaparin initiation.
• (100 anti-Xa IU equals 1 mg tinzaparin sodium.)

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Tinzaparin in adult patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Tinzaparin in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

There is limited information regarding Tinzaparin FDA-Labeled Indications and Dosage (Pediatric) in the drug label.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Tinzaparin in pediatric patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Tinzaparin in pediatric patients.

Contraindications

• Tinzaparin is contraindicated in patients with active major bleeding, in patients with (or history of) heparin-induced thrombocytopenia, or in patients with hypersensitivity to tinzaparin sodium.
• Patients with known hypersensitivity to heparin, sulfites, benzyl alcohol, or pork products should not be treated with tinzaparin.

Warnings

SPINAL/EPIDURAL HEMATOMAS See full prescribing information for complete Boxed Warning. Spinal/Epidural Hematomas: Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include: Use of indwelling epidural catheters Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants. A history of traumatic or repeated epidural or spinal punctures A history of spinal deformity or spinal surgery Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary. Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis

• INNOHEP® is not intended for intramuscular or intravenous administration.
• INNOHEP® cannot be used interchangeably (unit for unit) with heparin or other low molecular weight heparins as they differ in manufacturing process, molecular weight distribution, anti-Xa and anti-IIa activities, units, and dosage. Each of these medications has its own instructions for use.
• INNOHEP® should not be used in patients with a history of heparin-induced thrombocytopenia.

Increased Risk for Death in Elderly Patients with Renal Insufficiency

• INNOHEP® may increase the risk for death, compared to UFH, when administered to elderly patients with renal insufficiency.
• A clinical study compared INNOHEP® (175 IU/kg once daily; N = 269) and UFH (N = 268) in the initial treatment of deep vein thrombosis (DVT) and/or pulmonary embolism (PE) in elderly patients with renal insufficiency (i.e., patients aged 70 years or older with estimated creatinine clearance of ≤ 30 mL/min or patients aged 75 years or older with estimated creatinine clearance of ≤ 60 mL/min).
• Oral anticoagulants were co-administered beginning on Days 1-3 and study treatment was continued for at least five days until the international normalized ratio (INR) was between 2-3 on two successive days; oral anticoagulants were then continued alone and patients were followed until 90 days after the start of treatment.
• Overall mortality rates were 6.3% in patients treated with UFH and 11.5% in patients treated with INNOHEP®. Consider the use of alternatives to INNOHEP® in elderly patients with renal insufficiency.

Hemorrhage

• INNOHEP®, like other anticoagulants, should be used with extreme caution in conditions with increased risk of hemorrhage, such as bacterial endocarditis; severe uncontrolled hypertension; congenital or acquired bleeding disorders including hepatic failure and amyloidosis; active ulcerative and angiodysplastic gastrointestinal disease; hemorrhagic stroke; shortly after brain, spinal or ophthalmological surgery, or in patients treated concomitantly with platelet inhibitors.
• Bleeding can occur in any tissue or organ of the body during therapy with INNOHEP®. Hemorrhage in some cases has been reported to result in death or permanent disability.
• A hemorrhagic event should be seriously considered in the presence of an unexplained fall in hematocrit, hemoglobin, or blood pressure.
• If severe hemorrhage occurs, INNOHEP® should be discontinued.

• Spinal or epidural hematomas can occur with the associated use of low molecular weight heparins or heparinoids and spinal/epidural anesthesia or spinal puncture which can result in long-term or permanent paralysis. The risk of these events is higher with the use of post-operative indwelling epidural catheters or with the concomitant use of additional drugs affecting hemostasis such as NSAIDs.

Thrombocytopenia

• Thrombocytopenia can occur with the administration of INNOHEP®.
• In clinical studies, thrombocytopenia (platelet count <100,000/mm3 if baseline value ≥150,000/mm3, ≥50% decline if baseline <150,000/mm3) was identified in 1% of patients given INNOHEP®; severe thrombocytopenia (platelet count less than 50,000/mm3) occurred in 0.13%.
• Thrombocytopenia of any degree should be monitored closely.
• If the platelet count falls below 100,000/mm3, INNOHEP® should be discontinued. Cases of thrombocytopenia with disseminated thrombosis also have been observed in clinical practice with heparins, and low molecular weight heparins, including tinzaparin sodium. Some of these cases were complicated by organ infarction with secondary organ dysfunction or limb ischemia, and have resulted in death.

Hypersensitivity

• INNOHEP® contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening asthmatic episodes in certain susceptible people.
• The overall prevalence of sulfite sensitivity in the general population is unknown, but is probably low.
• Sulfite sensitivity is more frequent in asthmatic people than in non-asthmatic people.

Priapism

• Priapism has been reported from post-marketing surveillance as a rare occurrence. In some cases surgical intervention was required.

Miscellaneous

• INNOHEP® multiple dose vial contains benzyl alcohol as a preservative.
• The administration of medications containing benzyl alcohol as a preservative to premature neonates has been associated with a fatal “Gasping Syndrome."
• Because benzyl alcohol may cross the placenta, INNOHEP® preserved with benzyl alcohol should be used with caution in pregnant women only if clearly needed

Adverse Reactions

Clinical Trials Experience

There is limited information regarding Tinzaparin Clinical Trials Experience in the drug label.

Postmarketing Experience

There is limited information regarding Tinzaparin Postmarketing Experience in the drug label.

Drug Interactions

There is limited information regarding Tinzaparin Drug Interactions in the drug label.

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA): There is no FDA guidance on usage of Tinzaparin in women who are pregnant.
Pregnancy Category (AUS): There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Tinzaparin in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Tinzaparin during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Tinzaparin in women who are nursing.

Pediatric Use

There is no FDA guidance on the use of Tinzaparin in pediatric settings.

Geriatic Use

There is no FDA guidance on the use of Tinzaparin in geriatric settings.

Gender

There is no FDA guidance on the use of Tinzaparin with respect to specific gender populations.

Race

There is no FDA guidance on the use of Tinzaparin with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Tinzaparin in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Tinzaparin in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Tinzaparin in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Tinzaparin in patients who are immunocompromised.

Administration and Monitoring

Administration

There is limited information regarding Tinzaparin Administration in the drug label.

Monitoring

There is limited information regarding Tinzaparin Monitoring in the drug label.

IV Compatibility

There is limited information regarding the compatibility of Tinzaparin and IV administrations.

Overdosage

There is limited information regarding Tinzaparin overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.

Pharmacology

There is limited information regarding Tinzaparin Pharmacology in the drug label.

Mechanism of Action

There is limited information regarding Tinzaparin Mechanism of Action in the drug label.

Structure

There is limited information regarding Tinzaparin Structure in the drug label.

Pharmacodynamics

There is limited information regarding Tinzaparin Pharmacodynamics in the drug label.

Pharmacokinetics

There is limited information regarding Tinzaparin Pharmacokinetics in the drug label.

Nonclinical Toxicology

There is limited information regarding Tinzaparin Nonclinical Toxicology in the drug label.

Clinical Studies

There is limited information regarding Tinzaparin Clinical Studies in the drug label.

How Supplied

There is limited information regarding Tinzaparin How Supplied in the drug label.

Storage

There is limited information regarding Tinzaparin Storage in the drug label.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Tinzaparin Patient Counseling Information in the drug label.

Precautions with Alcohol

Alcohol-Tinzaparin interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

There is limited information regarding Tinzaparin Brand Names in the drug label.

Look-Alike Drug Names

There is limited information regarding Tinzaparin Look-Alike Drug Names in the drug label.

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

Tinzaparin

Clinical data
ATC code	B01AB10 (WHO)
Identifiers
CAS Number	9041-08-1
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}

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Clinical Trials
Ongoing Trials on Tinzaparin at Clinical Trials.gov Trial results on Tinzaparin Clinical Trials on Tinzaparin at Google
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3]