Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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14 branded products available
Part of the Micardis brand family (generic: Telmisartan + Hydrochlorothiazide)
MHRA licensed products
View all licensed products for Telmisartan + Hydrochlorothiazide on the MHRA register
MicardisPlus 40mg/12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
Telmisartan 40mg / Hydrochlorothiazide 12.5mg tablets
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 7 · Randomised trials: 11 · 1999–2026
Showing the 50 most relevant studies, sorted by most relevant.
Elbardisy S, Alotaibi MN, Saad AR, et al.
2024
Aggarwal P, Oza R, Solanki H, et al.
2025
Janet B. McGill, Paul A. Reilly
Clinical Therapeutics, 2001
- Telmisartan
- Angiotensin-Converting Enzyme Inhibitors
- Antihypertensive Agents
Y. Lacourciére, J. Neutel, H. Schumacher
Clinical therapeutics, 2005
- Telmisartan
- Antihypertensive Agents
- Benzimidazoles
Mapesi H, Rohacek M, Vanobberghen F, et al.
2025
- Hypertension
- Losartan
- Amlodipine
ImportanceHypertension is the primary cardiovascular risk factor in Africa. Recently revised World Health Organization guidelines recommend starting antihypertensive dual therapy; clinical efficacy and tolerability of low-dose triple combination remain unclear.ObjectivesTo compare the effect of 3 treatment strategies on blood pressure control among persons with untreated hypertension in Africa.Design, setting, and participantsThis was an open-label, parallel, 3-arm randomized clinical trial to evaluate noninferiority of a strategy starting 2 pills vs full-dose monotherapy with stepped escalation (noninferiority margin 10%) and superiority of starting low-dose 3 pills vs monotherapy allowing for monthly up titration. Recruitment lasted from March 5, 2020, to March 30, 2022. The setting was 2 hospitals in rural Lesotho and Tanzania. Participants included nonpregnant Black African individuals 18 years and older with uncomplicated, untreated hypertension (standardized office blood pressure ≥140 mm Hg systolic or ≥90 mm Hg diastolic).InterventionsParticipants were randomized 2:2:1 to stepped monotherapy (amlodipine, 10 mg, with escalation to add hydrochlorothiazide if needed), 2-pill strategy (amlodipine, 5 mg; losartan, 50 mg), or 3-pill strategy (amlodipine, 2.5 mg; losartan, 12.5 mg; hydrochlorothiazide, 6.25 mg). Drugs were up titrated monthly until reaching the target blood pressure (≤ 130/80 mm Hg for participants aged Main outcomes and measuresProportion of participants reaching target blood pressure at 12 weeks.ResultsOf 1761 participants screened, 1268 were enrolled (median [IQR] age, 54 [45-65] years; 914 female [72%]), with 505 in the monotherapy cohort, 510 in the 2-pill cohort, and 253 in the 3-pill cohort. In noninferiority analyses, 207 of 370 participants (56%) receiving the 2-pill strategy and 173 of 338 participants (51%) receiving the stepped monotherapy strategy achieved the blood pressure target (adjusted odds ratio [aOR], 1.18; 95% CI, 0.87-1.61), fulfilling noninferiority. In superiority analyses after multiple imputation for missing outcome data, 57% of participants receiving the 3-pill strategy, 55% receiving the 2-pill strategy, and 49% receiving the stepped monotherapy strategy reached the target blood pressure (aOR, 1.24; 95% CI, 0.94-1.63; P = .12 and aOR, 1.28; 95% CI, 0.91-1.79; P = .16 for the 2-pill and 3-pill vs stepped monotherapy strategies, respectively).Conclusions and relevanceResults of this randomized clinical trial show that in 2 African settings, for adults with uncomplicated untreated hypertension, a strategy starting a 2-pill low-dose treatment was noninferior to starting stepped monotherapy. Two-pill and 3-pill low-dose strategies were not superior to stepped monotherapy. Wide CIs preclude the ability to rule out potentially clinically important effects of the additional pill strategies for hypertension control.Trial registrationClinicalTrials.gov Identifier: NCT04129840.
Abstract licence: CC BY
Jia S, Zhang X, Yang X, et al.
2025
- Hypertension
- Reserpine
- Hydrochlorothiazide
Miriam Sharpe, Blair Jarvis, Karen L. Goa
Drugs, 2001
- Telmisartan
- Angiotensin II
- Angiotensin-Converting Enzyme Inhibitors
Puhong Zhang, Hongyi Wang, Lei Sun, et al.
Journal of Hypertension, 2017
Puhong Zhang, N. Sun, Hongyi Wang, et al.
Journal of hypertension, 2016
S Hillaert, W. Van den Bossche
Journal of Pharmaceutical and Biomedical Analysis, 2003
- Angiotensin Receptor Antagonists
- Angiotensin II
- Antihypertensive Agents
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.