Agranulocytosis Treatments
Find Agranulocytosis Treatments
Medications for Agranulocytosis
These are drugs that have been approved by the US Food and Drug Administration (FDA), meaning they have been determined to be safe and effective for use in Agranulocytosis.
Found 8 Approved Drugs for Agranulocytosis
Filgrastim
Brand Names
Granix, Neupogen, Nivestym, Nypozi, NYPOZI txid, Releuko, Zarxio
Filgrastim
Brand Names
Granix, Neupogen, Nivestym, Nypozi, NYPOZI txid, Releuko, Zarxio
Form: Injection
Method of administration: Subcutaneous, Intravenous
FDA approval date: April 07, 1997
Classification: Leukocyte Growth Factor
GRANIX is indicated to reduce the duration of severe neutropenia in adult and pediatric patients 1 month and older with non-myeloid malignancies receiving myelosuppressive anticancer drugs associated with a clinically significant incidence of febrile neutropenia. GRANIX (tbo-filgrastim) is a leukocyte growth factor indicated in adult and pediatric patients 1 month and older for reduction in the duration of severe neutropenia in patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs associated with a clinically significant incidence of febrile neutropenia. ( 1 )
Mavenclad
Generic Name
Cladribine
Mavenclad
Generic Name
Cladribine
Form: Injection, Tablet
Method of administration: Oral, Intravenous
FDA approval date: February 28, 2000
Classification: Purine Antimetabolite
MAVENCLAD is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include relapsing-remitting disease and active secondary progressive disease, in adults. Because of its safety profile, use of MAVENCLAD is generally recommended for patients who have had an inadequate response to, or are unable to tolerate, an alternate drug indicated for the treatment of MS. Limitations of Use MAVENCLAD is not recommended for use in patients with clinically isolated syndrome (CIS) because of its safety profile. MAVENCLAD is a purine antimetabolite indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include relapsing-remitting disease and active secondary progressive disease, in adults. Because of its safety profile, use of MAVENCLAD is generally recommended for patients who have had an inadequate response to, or are unable to tolerate, an alternate drug indicated for the treatment of MS. ( 1, 5 ) Limitations of Use MAVENCLAD is not recommended for use in patients with clinically isolated syndrome (CIS) because of its safety profile. ( 1, 5 )
Procainamide HCI
Generic Name
Procainamide
Procainamide HCI
Generic Name
Procainamide
Form: Injection
Method of administration: Intravenous, Intramuscular
FDA approval date: March 08, 2006
Classification: Antiarrhythmic
Procainamide hydrochloride injection is indicated for the treatment of documented ventricular arrhythmias, such as sustained ventricular tachycardia, that, in the judgement of the physician, are life-threatening. Because of the proarrhythmic effects of procainamide, its use with lesser arrhythmias is generally not recommended. Treatment of patients with asymptomatic ventricular premature contractions should be avoided. Initiation of procainamide treatment, as with other antiarrhythmic agents used to treat life-threatening arrhythmias, should be carried out in the hospital. Antiarrhythmic drugs have not been shown to enhance survival in patients with ventricular arrhythmias. Because procainamide has the potential to produce serious hematological disorders.
Nipent
Generic Name
Pentostatin
Nipent
Generic Name
Pentostatin
Form: Injection
Method of administration: Intravenous
FDA approval date: August 15, 2007
Classification: Nucleoside Metabolic Inhibitor
NIPENT is indicated as single-agent treatment for both untreated and alpha-interferon-refractory hairy cell leukemia patients with active disease as defined by clinically significant anemia, neutropenia, thrombocytopenia, or disease-related symptoms.
Lisinopril
Brand Names
Qbrelis, Zestoretic, Zestril
Lisinopril
Brand Names
Qbrelis, Zestoretic, Zestril
Form: Tablet, Solution
Method of administration: Oral
FDA approval date: July 01, 2002
Classification: Angiotensin Converting Enzyme Inhibitor
QBRELIS is an angiotensin converting enzyme (ACE) inhibitor indicated for: Treatment of hypertension in adults and pediatric patients 6 years of age and older.
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