Mechlorethamine (Systemic)
Name: Mechlorethamine (Systemic)
- Mechlorethamine Systemic used to treat
- Mechlorethamine Systemic is used to treat
- Mechlorethamine Systemic side effects
- Mechlorethamine Systemic effects of
- Mechlorethamine Systemic drug
- Mechlorethamine Systemic 10 mg
- Mechlorethamine Systemic injection
- Mechlorethamine Systemic uses
- Mechlorethamine Systemic dosage
- Mechlorethamine Systemic 1 mg
Uses of Mechlorethamine
- It is used to treat cancer.
- It may be given to you for other reasons. Talk with the doctor.
What are some other side effects of Mechlorethamine?
All drugs may cause side effects. However, many people have no side effects or only have minor side effects. Call your doctor or get medical help if any of these side effects or any other side effects bother you or do not go away:
- Loose stools (diarrhea).
- Not hungry.
- Upset stomach or throwing up.
- Feeling tired or weak.
These are not all of the side effects that may occur. If you have questions about side effects, call your doctor. Call your doctor for medical advice about side effects.
You may report side effects to the FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch.
Pronunciation
(me klor ETH a meen)
Dosage Forms
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.
Solution Reconstituted, Injection, as hydrochloride:
Mustargen: 10 mg (1 ea)
Use Labeled Indications
Hodgkin lymphoma: Palliative treatment of Hodgkin lymphoma
Malignant effusion: Palliative treatment of effusions from metastatic carcinomas
Additional approved uses (manufacturer labeling): Treatment of lymphosarcoma, chronic myelocytic or chronic lymphocytic leukemia, polycythemia vera, mycosis fungoides, and bronchogenic carcinoma
Dosing Hepatic Impairment
No dosage adjustment provided in manufacturer’s labeling.
The following have also been reported:
Mild-to-moderate impairment: No dosage adjustment necessary (Ecklund, 2005).
Severe liver impairment: No dosage adjustment necessary; concomitant chemotherapy may require alteration until improvement in hepatic function (Ecklund, 2005)
Reconstitution
Must be prepared immediately before use; degradation begins shortly after dilution. Dilute powder with 10 mL SWFI or NS to a final concentration of 1 mg/mL. May be further diluted in 50-100 mL NS for intracavitary administration.
Adverse Reactions
Frequency not defined.
Cardiovascular: Local thrombophlebitis
Central nervous system: Brain disease (high dose), drowsiness, headache, lethargy, metallic taste, sedation, vertigo
Dermatologic: Alopecia, diaphoresis, erythema multiforme, maculopapular rash, skin rash
Endocrine & metabolic: Amenorrhea, hyperuricemia, oligomenorrhea
Gastrointestinal: Anorexia, diarrhea, mucositis, nausea, vomiting
Genitourinary: Inhibition of spermatogenesis
Hepatic: Jaundice
Hematologic & oncologic: Agranulocytosis, granulocytopenia (onset: 6 to 8 days; recovery: 10 to 21 days), hemolytic anemia, leukopenia, lymphocytopenia, pancytopenia, petechia, thrombocytopenia
Hypersensitivity: Anaphylaxis, hypersensitivity reaction
Infection: Herpes zoster
Neuromuscular & skeletal: Weakness
Ophthalmic: Lacrimation
Otic: Deafness, tinnitus
Miscellaneous: Fever, tissue necrosis (extravasation)
Pregnancy Risk Factor D Pregnancy Considerations
Adverse events have been observed in animal reproduction studies. Women of childbearing potential are advised not to become pregnant during treatment. [U.S. Boxed Warning]: Avoid exposure during pregnancy.