Table 4.
ARV medication formulation | 2008 | 2011 | 2014 |
abacavir | P | ||
abacavir/lamivudine | P | X | |
atazanavir/ritonavir | X* | ||
didanosine | P | ||
efavirenz | X | X | X |
efavirenz/lamivudine/tenofovir | X | X | |
lamivudine | X | ||
lamivudine/nevirapine/stavudine | X | X | X |
lamivudine/nevirapine/zidovudine | X | X | |
lamivudine/stavudine | X | X | X |
lamivudine/tenofovir | X | X | |
lamivudine/zidovudine | X | X | X |
lopinavir/ritonavir | X | X | P** |
nevirapine | X | X | X |
tenofovir | X |
“X” indicates that a formulation was available in Malawi, while “P” indicates a medication that was available, but only for use in paediatric patients.
The atazanavir/ritonavir formulation became available in Malawi in April 2013, prior to the release of the 2014 guidelines.
Lopinavir/ritonavir is also available for treatment of adults with HIV and tuberculosis during simultaneous antiretroviral and rifampicin-based antituberculosis treatment.