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Strengths available for Dacogen injection:

Dacogen injection 50mg

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Latest news releases on Dacogen:

Dacogen (decitabine) FDA Approval History - Drugs.com

FDA approval history for Dacogen (decitabine) used to treat Myelodysplastic Diseases. Supplied by MGI Pharma Inc. and SuperGen Inc.

Dacogen: Uses, Dosage & Side Effects - Drugs.com

Dacogen (decitabine) is used to treat myelodysplastic syndromes (certain types of blood or bone marrow cancer). Includes Dacogen side effects, interactions and ...

DACOGEN. ------------------------------ CONTRAINDICATIONS

FULL PRESCRIBING INFORMATION . 1 INDICATIONS AND USAGE DACOGEN is indicated for treatment of patients with myelodysplastic syndromes adult (MDS) including previously ...

Dacogen (Decitabine Injection): Side Effects, Interactions ...

Learn about Dacogen (Decitabine Injection) may treat, uses, dosage, side effects, drug interactions, warnings, patient labeling, reviews, and related medications.

Common Side Effects of Dacogen (Decitabine Injection) Drug ...

Find a comprehensive guide to possible side effects including common and rare side effects when taking Dacogen (Decitabine Injection) for healthcare professionals and ...

Dacogen ® - compendium.ch

Posologie/Mode d’emploi. Dacogen doit être administré sous la surveillance d'un médecin expérimenté dans l'utilisation de la chimiothérapie.

Dacogen 50 mg powder for concentrate for solution for ...

Dacogen 50 mg powder for concentrate for solution for infusion. - Summary of Product Characteristics (SmPC) by Janssen-Cilag Ltd

Dacogen (decitabine) dose, indications, adverse effects ...

PDR Drug Summaries are concise point-of-care prescribing, dosing and administering information to help phsyicans more efficiently and accurately prescribe in their ...

Drug Approval Package: Dacogen (Decitabine) NDA #021790

Drug Review Package ... 10903 New Hampshire Avenue Silver Spring, MD 20993 Ph. 1-888-INFO-FDA (1-888-463-6332) Contact FDA

An Efficacy and Safety Study of Decitabine (DACOGEN) Plus ...

The primary objective of study Part A is to assess the safety of talacotuzumab (formerly CSL362) monotherapy and confirm the recommended Phase 2 dose (RP2D) in ...

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