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SPP Brand names, SPP Analogs

SPP Brand Names Mixture

  • No information avaliable

SPP Chemical_Formula

C22H28N6O3S

SPP RX_link

No information avaliable

SPP fda sheet

SPP FDA

SPP msds (material safety sheet)

SPP Synthesis Reference

D. L. Romero et al., PCT Int. pat. Appl. 91 09,849 (1991)

SPP Molecular Weight

456.562 g/mol

SPP Melting Point

226-228 oC

SPP H2O Solubility

No information avaliable

SPP State

Solid

SPP LogP

2.926

SPP Dosage Forms

Caplet

SPP Indication

For the treatment of HIV-1 infection in combination with appropriate antiretroviral agents when therapy is warranted

SPP Pharmacology

Delavirdine is a non-nucleoside reverse transcriptase inhibitor (nNRTI) with activity against Human Immunodeficiency Virus Type 1 (HIV-1). Delavirdine binds directly to reverse transcriptase (RT) and blocks the RNA-dependent and DNA-dependent DNA polymerase activities by causing a disruption of the enzyme's catalytic site. The activity of Delavirdine does not compete with template or nucleoside triphosphates. HIV-2 RT and eukaryotic DNA polymerases (such as human DNA polymerases alpha, beta, or sigma) are not inhibited by Delavirdine.

SPP Absorption

Rapidly absorbed

SPP side effects and Toxicity

Major toxicity of delavirdine is rash and should be advised to promptly notify their physician should rash occur. The majority of rashes associated with delavirdine occur within 1 to 3 weeks after initiating treatment with delavirdine. The rash normally resolves in 3 to 14 days and may be treated symptomatically while therapy with delavirdine is continued. Any patient experiencing severe rash or rash accompanied by symptoms such as fever, blistering, oral lesions, conjunctivitis, swelling, muscle or joint aches should discontinue medication and consult a physician.

SPP Patient Information

Patients should be informed that RESCRIPTOR is not a cure for HIV-1
infection and that they may continue to acquire illnesses associated
with HIV-1 infection, including opportunistic infections. Treatment
with RESCRIPTOR has not been shown to reduce the incidence or frequency
of such illnesses, and patients should be advised to remain under the
care of a physician when using RESCRIPTOR. Patients should be advised
that the long-term effects of treatment with RESCRIPTOR are unknown at
this time. They should be advised that the use of RESCRIPTOR has not been
shown to reduce the risk of transmission of HIV-1.

SPP Organisms Affected

Human immunodeficiency virus