Evidence map›Paper›PMID 41803456›Full record

ArticleScientific reports2026

Post-market surveillance of antiretroviral drug quality in Tanzania in the context of rising HIV drug resistance.

Eulambius M Mlugu, Jacob B Mhagama, Raphael Zozimus Sangeda, Peter P Kunambi, Thomas Samwel, Nellin Shiletiwa, Goodluck Gotora, Sunzy M Chambiri, Damas Matiko, Danstan Hipolite and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Eulambius M MluguDepartment of Pharmaceutics and Pharmacy Practice, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania. mlugusonlove@gmail.com.
Jacob B MhagamaTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Raphael Zozimus SangedaDepartment of Pharmaceutical Microbiology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Peter P KunambiDepartment of Clinical Pharmacology, School of Biomedical Sciences, Campus College of Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Thomas SamwelTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Nellin ShiletiwaTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Goodluck GotoraTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Sunzy M ChambiriTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Damas MatikoTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Danstan HipoliteTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Yonah H MwalwisiTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.
Adam Mitangu FimboTanzania Medicines and Medical Devices Authority (TMDA), Dodoma, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human Immunodeficiency Virus (HIV) remains a major global health burden. Antiretroviral (ARV) drugs play a key role in the control of HIV. However, their effectiveness could be affected by poor-quality drugs, risking treatment failure and HIV drug resistance (HIVDR). Reports on the quality of ARV drugs from sub-Saharan Africa remain low despite the growing threat of HIVDR. This study presents Tanzanian post-market surveillance (PMS) data on ARV quality, offering evidence to strengthen monitoring systems and inform HIV/AIDS control strategies. This was a descriptive cross-sectional study conducted across 15 regions of mainland Tanzania. ARVs were randomly sampled from the port of entry and distribution outlets. All samples underwent Tier I screening, which included visual inspection, disintegration tests, and Thin Layer Chromatography using a Global Pharma Health Fund Minilab. Samples from the distribution outlet were also subjected to product information review (PIR). All samples that failed Tier I screening, irrespective of their source, were subjected to Tier II confirmatory testing using standard methods. In addition, 10% of samples from distribution outlets that passed Tier I screening were randomly selected for Tier II confirmatory testing in accordance with the national PMS guideline. Samples were considered to pass if the test results complied with the standard pharmacopeia acceptance criteria. A total of 1432 ARV samples were collected from July 2019 to December 2023. Of these, 81.8% (1171/1432) were collected from the port of entry. The first line combination (dolutegravir + lamivudine + tenofovir disoproxil fumarate) comprised about two-thirds (68%) of the screened samples. Nearly half (49.4%) of ARVs from the distribution outlets did not comply with the PIR requirements of the approved product information. Failure to comply with the PIR requirement risks the public health, safety and effective use of ARVs. All samples passed Tier I and Tier II tests. This study demonstrates that ARVs circulating in Tanzania meet the required quality standards; however, the observed labeling deviations necessitate urgent corrective action. In light of rising HIVDR, continuous quality surveillance remains essential.

Indexed as

Anti-HIV AgentsAnti-Retroviral AgentsDrug Resistance, ViralHIV InfectionsProduct Surveillance, PostmarketingCross-Sectional StudiesHIV-1HumansTanzaniaAnti-HIV AgentsAnti-Retroviral AgentsAntiretroviral drugsHIV drug resistancePost-market surveillanceQuality

Identifiers

PMID41803456
PMCPMC13096481

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.