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Bolemide (Pomalidomide) 2mg

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Model Number：

RL142023090179
Brand Name：

Bolemide
Origin：

Generic drug, LAOS.
Small Orders：

Small order has available
Tags：

Multiple Myeloma

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Details
Description

Packaging Size

2mg*21Capsules/Box
Strength

2mg
Compositon

Pomalidomide
Treatment

multiple myeloma
Form

Capsule
Brand

Bolemide
Quantity Unit

21Capsules/Box
Manufacturer

Tongmeng (Lao) Pharmaceutical & Food Co., Ltd.（TLPH）

Contents hide

1 Indications

2 Dosage and Administration

3 Warnings and Precautions

4 Adverse reactions

Indications

Permalidomide is a thalidomide analog in combination with dexamethasone for patients with multiple myeloma who have received at least two prior therapies , including lenalidomide and a proteasome inhibitor , and who have been Disease progression was confirmed within 60 days of completion of the last treatment .

Dosage and Administration

1. Administration

Multiple myeloma : pomalidomide 4 mg orally per day on days 1-21 of a cycle of 28 days ;

In combination with 40 mg daily on days 1 , 8 , 15, and 22 of each cycle ; more than

For 75-year-olds, the initial dose of dexamethasone is daily on days 1 , 8, 15, and 22 of each cycle.

2 0mg each time. Cycles are repeated until disease progression or toxicity is not tolerated.

2. Dosage Form Specifications

● Capsules, 2 mg, 3 mg, 4 mg. 3. Contraindications: Pregnant women are prohibited .

Warnings and Precautions

● Hematologic toxicity : The most common grade 3/4 adverse event was neutropenia . Monitor patients for hematologic toxicity , especially neutropenia .

• Hepatotoxicity: Liver failure including fatal events; monitor liver function tests monthly .

● Hypersensitivity reactions : Angioedema and severe dermatological reactions have been reported . vascular water

Swelling and severe dermatological reactions discontinue pomalidomide therapy .

Tumor lysis syndrome (TLS ) : monitor patients at risk for TLS (eg , patients with high tumor burden)

) and take appropriate precautions .

Adverse reactions

The most common adverse reactions ( ≥ 30%) : fatigue, asthenia , neutropenia , anemia , constipation , nausea , diarrhea , dyspnea, upper respiratory tract infection , back pain and fever .