{"id":51694,"date":"2023-09-20T09:24:29","date_gmt":"2023-09-20T09:24:29","guid":{"rendered":"https:\/\/medsname.com\/dilvas\/"},"modified":"2026-05-01T10:49:11","modified_gmt":"2026-05-01T10:49:11","slug":"dilvas","status":"publish","type":"product","link":"https:\/\/medsbase.com\/dilvas\/","title":{"rendered":"Dilvas"},"content":{"rendered":"<p><!-- medsbase-tldr-answer --><\/p>\n<div style=\"background:#fff8e1;border-left:4px solid #f5a623;padding:18px 22px;margin:0 0 24px 0;border-radius:4px;\">\n<h3 class=\"wp-block-heading\" style=\"margin:0 0 8px 0;font-size:16px;font-weight:700;\">&#9889; Quick Answer &mdash; What is Dilvas?<\/h3>\n<p style=\"margin:0;\"><strong>Dilvas<\/strong> is a <strong>2.5 \/ 5 \/ 10 mg enalapril tablet<\/strong> from a WHO-GMP certified manufacturer &mdash; an <strong>angiotensin-converting enzyme (ACE) inhibitor<\/strong>. ACE inhibitors are <strong>first-line antihypertensive therapy<\/strong> in most international guidelines (NICE, AHA\/ACC, ESC\/ESH), particularly for patients under 55 and for diabetics, heart-failure patients, post-MI patients, and those with proteinuric kidney disease. Enalapril is a <strong>prodrug<\/strong> converted in the liver to enalaprilat (the active ACE inhibitor) with effective half-life 11 hours (enalaprilat) &mdash; usually once-daily; occasionally divided twice daily. Typical hypertension dose: <strong>start 5 mg once daily (2.5 mg if elderly, renal impaired, volume depleted, or on a diuretic), titrate to 10-20 mg once daily<\/strong>. Main side effect: <strong>dry persistent cough<\/strong> (up to 20% of users, class effect; if intolerable, switch to an ARB such as <a href=\"https:\/\/medsbase.com\/losar\/\">losartan<\/a> or <a href=\"https:\/\/medsbase.com\/telmaheal\/\">telmisartan<\/a>). Other class effects: hyperkalaemia, first-dose hypotension, reversible rise in creatinine at start. <strong>Absolutely contraindicated in pregnancy<\/strong> (all trimesters &mdash; causes fetal renal agenesis, oligohydramnios, pulmonary hypoplasia, skull defects), bilateral renal artery stenosis, and history of ACE-inhibitor-induced angioedema.<\/p>\n<\/div>\n<div class=\"medsbase-trust-strip\" style=\"background:#f4f8fb;border:1px solid #d8e3eb;padding:12px 16px;margin:16px 0;border-radius:4px;font-size:14px;\">\n<strong>What you get with MedsBase:<\/strong> WHO-GMP certified manufacturer \u00b7 Discreet packaging \u00b7 Worldwide shipping \u00b7 1,400+ verified <a href=\"https:\/\/medsbase.com\/reviews\/\">customer reviews<\/a>\n<\/div>\n<p class=\"medsbase-reship-line\" style=\"font-size:14px;color:#444;margin:8px 0 18px;\">\ud83d\udce6 Every order is covered by our <a href=\"https:\/\/medsbase.com\/medsbase-re-shipment-assurance-policy\/\"><strong>Reshipment Assurance Policy<\/strong><\/a> \u2014 if your parcel does not arrive within 20 business days, we reship it.<\/p>\n<h3>Why order from MedsBase<\/h3>\n<p>Our generic medications are sourced from WHO-GMP certified manufacturers and shipped worldwide in discreet, plain packaging \u2014 no medication name on the parcel exterior. Card payments are routed through a regulated processor (statement descriptors include a regulated card-payment processor \u2014 never &ldquo;MedsBase&rdquo; or any medication name). Crypto and SEPA bank transfer are also accepted. Every order is backed by our Reshipment Assurance Policy.<\/p>\n<h2 class=\"wp-block-heading\">What Is Dilvas?<\/h2>\n<p>Dilvas is an oral 2.5 \/ 5 \/ 10 mg enalapril tablet from a WHO-GMP certified manufacturer, supplied in 30-90 tablets. Introduced 1984 as <strong>Vasotec \/ Renitec<\/strong> (MSD) &mdash; the second ACE inhibitor ever marketed after captopril, and the first oral once-daily agent in the class.<\/p>\n<p>Enalapril is a <strong>prodrug<\/strong> converted in the liver to enalaprilat (the active ACE inhibitor), with effective half-life 11 hours (enalaprilat) &mdash; usually once-daily; occasionally divided twice daily.<\/p>\n<h2 class=\"wp-block-heading\">How Enalapril Lowers Blood Pressure<\/h2>\n<p>ACE inhibitors block the <strong>angiotensin-converting enzyme<\/strong>, which catalyses the conversion of inactive angiotensin I to active angiotensin II. Angiotensin II is a potent vasoconstrictor and the primary stimulus for adrenal aldosterone release. Blocking its formation produces:<\/p>\n<ul>\n<li><strong>Direct arterial vasodilation<\/strong> &mdash; reduced systemic vascular resistance = lower blood pressure<\/li>\n<li><strong>Reduced aldosterone secretion<\/strong> &mdash; less renal sodium and water retention<\/li>\n<li><strong>Reduced preload<\/strong> (venous + modest ventricular unloading) &mdash; particularly important in heart failure<\/li>\n<li><strong>Bradykinin accumulation<\/strong> &mdash; ACE also degrades bradykinin; blocking ACE raises bradykinin levels, which potentiates vasodilation (and causes the dry-cough side effect in ~20% of users)<\/li>\n<li><strong>Reduced sympathetic nervous system activation<\/strong><\/li>\n<li><strong>Endothelial function improvement<\/strong> and reduced ventricular remodelling &mdash; responsible for the vascular-protective effects seen in trials (HOPE, EUROPA) that extend beyond BP lowering alone<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Approved and Evidence-Based Uses<\/h2>\n<ul>\n<li><strong>Hypertension<\/strong> &mdash; primary indication, first-line per NICE, ESC\/ESH, and AHA\/ACC guidelines for most adults under 55 and for all ages with diabetes, CKD, or heart failure<\/li>\n<li><strong>Heart failure with reduced ejection fraction (HF-REF)<\/strong> &mdash; foundational mortality evidence (CONSENSUS, SOLVD)<\/li>\n<li><strong>Asymptomatic left-ventricular dysfunction<\/strong><\/li>\n<li><strong>Diabetic nephropathy<\/strong><\/li>\n<li><strong>Proteinuric chronic kidney disease<\/strong><\/li>\n<\/ul>\n<p><strong>Pivotal trial evidence:<\/strong> CONSENSUS trial (1987) &mdash; enalapril reduced mortality by 40% in NYHA class IV heart failure. SOLVD trial &mdash; mortality and hospitalisation reduction in HF-REF. These were the two first large-scale demonstrations that ACE inhibitors save lives in heart failure, establishing the class as cornerstone therapy.<\/p>\n<h2 class=\"wp-block-heading\">Dilvas Dosage<\/h2>\n<p><strong>Hypertension:<\/strong><\/p>\n<ul>\n<li><strong>Starting dose:<\/strong> 5 mg once daily (2.5 mg if elderly, renal impaired, volume depleted, or on a diuretic)<\/li>\n<li><strong>Target dose:<\/strong> 10-20 mg once daily<\/li>\n<li><strong>Maximum:<\/strong> 40 mg\/day (usually divided BD if using at higher end)<\/li>\n<li>Titrate every 2-4 weeks based on BP response and tolerability<\/li>\n<\/ul>\n<p><strong>Heart failure with reduced ejection fraction (HF-REF):<\/strong> Start 2.5 mg twice daily; titrate to 10-20 mg twice daily (HF-REF target)<\/p>\n<p><strong>Post-myocardial infarction:<\/strong> 2.5-20 mg\/day<\/p>\n<p><strong>First-dose precautions:<\/strong> first-dose hypotension is most likely in patients on high-dose diuretics, in dehydrated patients, in heart failure, and in elderly patients. Take the first dose at bedtime; monitor BP; hold diuretics for 24-48 hours before starting if possible.<\/p>\n<p><strong>Monitoring:<\/strong><\/p>\n<ul>\n<li>Baseline: urea, electrolytes (especially potassium), creatinine, eGFR. Get a blood pressure baseline.<\/li>\n<li>After 1-2 weeks: repeat U&amp;E. Expected effects: small rise in creatinine (up to 30% is acceptable and reflects intrarenal haemodynamic change, not nephrotoxicity); small rise in potassium.<\/li>\n<li>After dose increase: repeat U&amp;E at 1-2 weeks.<\/li>\n<li>Ongoing: annual U&amp;E once stable.<\/li>\n<li><strong>Stop and investigate:<\/strong> creatinine rise &gt;30%, eGFR fall &gt;25%, potassium &gt;5.5, new hypotension \/ dizziness.<\/li>\n<\/ul>\n<p><strong>Discontinuation:<\/strong> tapering is not strictly required for ACE inhibitors (unlike beta-blockers), but abrupt discontinuation causes BP rebound within days. If stopping, taper over 1-2 weeks and monitor BP.<\/p>\n<h2 class=\"wp-block-heading\">Side Effects<\/h2>\n<p><strong>Common (&gt;5%):<\/strong><\/p>\n<ul>\n<li><strong>Dry persistent cough<\/strong> (up to 20% &mdash; class effect due to bradykinin accumulation). Usually starts within weeks of beginning therapy; does not go away with time. If troublesome, switch to an ARB (losartan, telmisartan, olmesartan, valsartan, irbesartan) &mdash; ARBs do not cause cough because they act downstream of bradykinin metabolism.<\/li>\n<li>Dizziness, postural hypotension (particularly at start of therapy)<\/li>\n<li>Mild hyperkalaemia (check potassium)<\/li>\n<li>Reversible rise in serum creatinine (up to ~30% is expected and acceptable)<\/li>\n<li>Headache, fatigue<\/li>\n<li>Altered taste sensation (dysgeusia)<\/li>\n<\/ul>\n<p><strong>Uncommon but important:<\/strong><\/p>\n<ul>\n<li><strong>Angioedema<\/strong> &mdash; potentially life-threatening swelling of lips, tongue, airway. Incidence ~0.1-0.5%; higher in patients of African descent. Can occur after years of uneventful use. <strong>Stop immediately<\/strong>, seek emergency care, and do not restart any ACE inhibitor &mdash; also contraindicated for ARBs in first 4 weeks in patients with ACEi angioedema history.<\/li>\n<li><strong>Acute kidney injury in bilateral renal artery stenosis<\/strong> &mdash; ACE inhibition removes the angiotensin-II-dependent efferent arteriolar constriction that maintains GFR in severely compromised renal perfusion. Usually reveals itself as a &gt;30% creatinine rise within days of starting.<\/li>\n<li><strong>Severe hyperkalaemia<\/strong> &mdash; particularly with potassium supplements, potassium-sparing diuretics (spironolactone), NSAIDs, or in CKD<\/li>\n<li><strong>Neutropenia and agranulocytosis<\/strong> &mdash; very rare, mostly a historical concern from captopril<\/li>\n<li><strong>Hepatic dysfunction \/ cholestatic jaundice<\/strong> &mdash; very rare<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Contraindications<\/h2>\n<ul>\n<li><strong>Pregnancy &mdash; ABSOLUTE contraindication at all trimesters.<\/strong> ACE inhibitors cause fetal renal agenesis, oligohydramnios, pulmonary hypoplasia, and skull hypoplasia. Stop immediately if pregnancy occurs. Women of childbearing potential should use reliable contraception or switch to a pregnancy-safe antihypertensive (<a href=\"https:\/\/medsbase.com\/labebet\/\">labetalol<\/a>, methyldopa, nifedipine, hydralazine) before conception.<\/li>\n<li><strong>History of ACE-inhibitor-induced angioedema<\/strong> &mdash; absolute; even a single past episode makes ACE inhibitors contraindicated for life<\/li>\n<li><strong>Bilateral renal artery stenosis<\/strong> or stenosis in a single functioning kidney &mdash; AKI risk<\/li>\n<li><strong>Hereditary or idiopathic angioedema<\/strong><\/li>\n<li><strong>Severe aortic stenosis<\/strong> &mdash; relative; can precipitate hypotension<\/li>\n<li><strong>Hyperkalaemia &gt;5.5 mmol\/L<\/strong> at baseline (correct first)<\/li>\n<li><strong>Concurrent sacubitril \/ valsartan (Entresto)<\/strong> &mdash; do not combine; 36-hour washout required<\/li>\n<li><strong>Concurrent aliskiren in diabetes or CKD<\/strong> (direct renin inhibitor)<\/li>\n<li>Hypersensitivity to enalapril<\/li>\n<\/ul>\n<p><strong>Breastfeeding:<\/strong> enalapril and captopril are considered compatible (small amounts in breast milk); data for enalapril is limited &mdash; avoid in the first weeks after delivery of a premature infant; generally acceptable thereafter.<\/p>\n<h2 class=\"wp-block-heading\">Drug Interactions<\/h2>\n<ul>\n<li><strong>Potassium-sparing diuretics<\/strong> (spironolactone, eplerenone, amiloride, triamterene) &mdash; additive hyperkalaemia; monitor K<sup>+<\/sup> closely. The combination is clinically used in HF-REF but requires careful monitoring.<\/li>\n<li><strong>Potassium supplements<\/strong> and salt substitutes containing potassium &mdash; hyperkalaemia risk<\/li>\n<li><strong>NSAIDs<\/strong> (ibuprofen, diclofenac, naproxen) &mdash; reduce the antihypertensive effect of ACE inhibitors AND increase AKI risk (&ldquo;triple whammy&rdquo; = ACEi + diuretic + NSAID). Avoid chronic combination.<\/li>\n<li><strong>Lithium<\/strong> &mdash; ACE inhibitors reduce renal lithium clearance; monitor lithium levels closely<\/li>\n<li><strong>Other antihypertensives<\/strong> &mdash; usually complementary; monitor BP<\/li>\n<li><strong>Sacubitril\/valsartan (Entresto)<\/strong> &mdash; do not combine; 36-hour washout required to avoid angioedema risk<\/li>\n<li><strong>Allopurinol<\/strong> &mdash; rare reports of increased hypersensitivity; clinically minor<\/li>\n<li><strong>Aliskiren<\/strong> &mdash; avoid combination in diabetes and CKD (ALTITUDE trial stopped early for harm)<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">ACE Inhibitor Class at a Glance<\/h2>\n<table style=\"width:100%;border-collapse:collapse;margin:14px 0;\">\n<thead>\n<tr style=\"background:#2c7cb0;color:#fff;\">\n<th style=\"padding:10px;border:1px solid #ddd;text-align:left;\">ACE Inhibitor<\/th>\n<th style=\"padding:10px;border:1px solid #ddd;text-align:left;\">Activation<\/th>\n<th style=\"padding:10px;border:1px solid #ddd;text-align:left;\">Best for \/ key trial<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td style=\"padding:10px;border:1px solid #ddd;\"><a href=\"https:\/\/medsbase.com\/ramcor\/\">Ramipril (Ramcor, Rami Race, Ramgee, Ramisave)<\/a><\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Prodrug (liver &rarr; ramiprilat)<\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Vascular protection (HOPE); post-MI (AIRE)<\/td>\n<\/tr>\n<tr style=\"background:#fff3cd;\">\n<td style=\"padding:10px;border:1px solid #ddd;\"><a href=\"https:\/\/medsbase.com\/enapril\/\">Enalapril (Enapril)<\/a><\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Prodrug (liver &rarr; enalaprilat)<\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Heart failure (CONSENSUS, SOLVD)<\/td>\n<\/tr>\n<tr>\n<td style=\"padding:10px;border:1px solid #ddd;\"><a href=\"https:\/\/medsbase.com\/lispro\/\">Lisinopril (Lispro, Hypernil)<\/a><\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Active drug (no liver needed)<\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Preferred in hepatic impairment; HF (ATLAS); post-MI (GISSI-3)<\/td>\n<\/tr>\n<tr style=\"background:#f9f9f9;\">\n<td style=\"padding:10px;border:1px solid #ddd;\"><a href=\"https:\/\/medsbase.com\/coversyl\/\">Perindopril (Coversyl)<\/a><\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Prodrug (liver &rarr; perindoprilat)<\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Longest half-life; HTN (ASCOT-BPLA); CAD (EUROPA); stroke prevention (PROGRESS)<\/td>\n<\/tr>\n<tr>\n<td style=\"padding:10px;border:1px solid #ddd;\">Captopril<\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Active drug<\/td>\n<td style=\"padding:10px;border:1px solid #ddd;\">Short half-life (6 h); historical reference agent; rarely first-line now<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2 class=\"wp-block-heading\">ACE Inhibitor vs ARB &mdash; Which to Use?<\/h2>\n<p>Angiotensin receptor blockers (ARBs &mdash; <a href=\"https:\/\/medsbase.com\/losar\/\">losartan<\/a>, <a href=\"https:\/\/medsbase.com\/telmaheal\/\">telmisartan<\/a>, <a href=\"https:\/\/medsbase.com\/olmin\/\">olmesartan<\/a>, valsartan, irbesartan) work on the same renin-angiotensin pathway but block angiotensin II at its AT1 receptor rather than blocking its formation. Clinical effect on BP is broadly equivalent. Differences:<\/p>\n<ul>\n<li><strong>No dry cough<\/strong> with ARBs &mdash; they don&#8217;t raise bradykinin levels. ARBs are the first choice after ACEi cough.<\/li>\n<li><strong>Angioedema is rare but possible with ARBs<\/strong> &mdash; do NOT start an ARB within 4 weeks of an ACEi-angioedema episode; longer-term ARB use in previous ACEi-angioedema patients is generally acceptable but monitored.<\/li>\n<li><strong>Cost<\/strong> &mdash; generic ACE inhibitors are slightly cheaper than generic ARBs in most markets<\/li>\n<li><strong>Heart failure evidence<\/strong> &mdash; ACE inhibitors have slightly stronger historical mortality evidence; ARBs are validated as equivalent in more recent trials and used when ACEi is not tolerated<\/li>\n<li><strong>Do NOT combine ACEi + ARB<\/strong> &mdash; ONTARGET trial showed harm (more hyperkalaemia, AKI, hypotension) without additional mortality benefit<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\">Storage<\/h2>\n<p>Store Dilvas below 25&deg;C in the original blister pack. Protect from moisture. Keep out of reach of children.<\/p>\n<h2 id=\"faqs\">Frequently Asked Questions<\/h2>\n<h3 class=\"wp-block-heading\">How long does Dilvas take to lower blood pressure?<\/h3>\n<p>Initial BP drop within 1-2 hours of the first dose; full antihypertensive effect at 2-4 weeks as the renin-angiotensin system fully adjusts. Measure home BP at the same time each day to track response.<\/p>\n<h3 class=\"wp-block-heading\">Why did I develop a cough after starting Dilvas?<\/h3>\n<p>ACE inhibitors raise bradykinin levels in the respiratory tract, causing a characteristic <strong>dry, persistent cough in up to 20% of users<\/strong>. It usually starts within days to weeks, does not improve with antitussives, and does not resolve while continuing the drug. If the cough is bothersome, switch to an ARB (<a href=\"https:\/\/medsbase.com\/losar\/\">losartan<\/a>, <a href=\"https:\/\/medsbase.com\/telmaheal\/\">telmisartan<\/a>, <a href=\"https:\/\/medsbase.com\/olmin\/\">olmesartan<\/a>) &mdash; the cough resolves within 1-4 weeks of stopping the ACE inhibitor.<\/p>\n<h3 class=\"wp-block-heading\">Can I take Dilvas in pregnancy?<\/h3>\n<p><strong>No &mdash; ACE inhibitors are absolutely contraindicated in pregnancy.<\/strong> They cause fetal renal agenesis, oligohydramnios, pulmonary hypoplasia, and skull hypoplasia. Stop immediately if pregnancy occurs and switch to a pregnancy-safe antihypertensive &mdash; <a href=\"https:\/\/medsbase.com\/labebet\/\">labetalol<\/a>, methyldopa, nifedipine, or hydralazine. Women of childbearing potential should use reliable contraception.<\/p>\n<h3 class=\"wp-block-heading\">My creatinine went up after starting Dilvas &mdash; should I stop?<\/h3>\n<p>A <strong>creatinine rise of up to 30%<\/strong> within the first 1-2 weeks is <strong>expected<\/strong> and acceptable &mdash; it reflects intrarenal haemodynamic adjustment as the angiotensin-II-dependent efferent arteriolar constriction is removed, not nephrotoxicity. A rise of &gt;30% suggests possible bilateral renal artery stenosis, volume depletion, or NSAID interaction &mdash; stop the drug and investigate.<\/p>\n<h3 class=\"wp-block-heading\">Can I drink alcohol on Dilvas?<\/h3>\n<p>Moderate alcohol is generally acceptable but alcohol is additive with the vasodilator effect &mdash; you may feel dizzy on standing up after drinking. Heavy drinking also independently raises BP; reducing alcohol often improves BP control independent of Dilvas.<\/p>\n<h3 class=\"wp-block-heading\">Should I avoid potassium-rich foods on Dilvas?<\/h3>\n<p>Moderate intake of potassium-rich foods (bananas, oranges, spinach, avocado) is fine for most patients. Avoid potassium supplements (slow-K tablets) and salt substitutes containing potassium chloride unless specifically prescribed &mdash; these can cause dangerous hyperkalaemia when combined with ACE inhibitors, particularly in CKD or with potassium-sparing diuretics.<\/p>\n<h3 class=\"wp-block-heading\">Can I take ibuprofen while on Dilvas?<\/h3>\n<p>Occasional short-term NSAID use is usually acceptable, but <strong>chronic daily NSAIDs<\/strong> (ibuprofen, diclofenac, naproxen) reduce the antihypertensive effect of ACE inhibitors AND substantially raise the AKI risk &mdash; particularly when combined with a diuretic (&ldquo;triple whammy&rdquo; = ACEi + diuretic + NSAID). For chronic pain, paracetamol is safer; for inflammation, discuss alternatives with your doctor.<\/p>\n<h3 class=\"wp-block-heading\">Can I take Dilvas with my other BP medications?<\/h3>\n<p>Yes &mdash; ACE inhibitors combine well with <strong>calcium-channel blockers<\/strong> (<a href=\"https:\/\/medsbase.com\/amlode\/\">amlodipine<\/a>, nifedipine), <strong>thiazide diuretics<\/strong> (<a href=\"https:\/\/medsbase.com\/aquazide\/\">HCTZ<\/a>, indapamide), <strong>beta-blockers<\/strong> (<a href=\"https:\/\/medsbase.com\/concor\/\">bisoprolol<\/a>, <a href=\"https:\/\/medsbase.com\/betablock-xl\/\">metoprolol<\/a>), and <strong>aldosterone antagonists<\/strong> (spironolactone &mdash; monitor K<sup>+<\/sup>). <strong>Do not combine with an ARB<\/strong> (ONTARGET trial showed harm with no benefit).<\/p>\n<h3 class=\"wp-block-heading\">What if I miss a dose?<\/h3>\n<p>Take it as soon as you remember, unless it is nearly time for the next dose &mdash; in that case skip the missed dose and continue your normal schedule. Do not double up. A single missed dose won&#8217;t meaningfully affect BP control because ACE inhibitors have long-lasting pharmacological effects via tissue binding.<\/p>\n<h3 class=\"wp-block-heading\">Where can I buy Dilvas online?<\/h3>\n<p>You can buy Dilvas (enalapril 2.5 \/ 5 \/ 10 mg, 30-90 tablets) from MedsBase with discreet packaging and worldwide shipping.<\/p>\n<h2 class=\"wp-block-heading\">Related Antihypertensives on MedsBase<\/h2>\n<ul>\n<li><a href=\"https:\/\/medsbase.com\/amlode\/\">Amlode &mdash; Amlodipine CCB<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/concor\/\">Concor &mdash; Bisoprolol 5\/10 mg<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/lispro\/\">Lispro &mdash; Lisinopril 2.5\/5\/10 mg<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/listril-plus\/\">Listril Plus &mdash; Lisinopril + HCTZ combo<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/rami-race\/\">Rami Race &mdash; Ramipril 10 mg<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/telmaheal\/\">Telmaheal &mdash; Telmisartan (ARB alternative)<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/high-blood-pressure-medication\/\"><strong>Browse all High Blood Pressure Medications<\/strong><\/a><\/li>\n<\/ul>\n<div style=\"background:#fff3f3;border-left:4px solid #d9534f;padding:16px 20px;margin:24px 0;border-radius:4px;\"><strong>&#9877; Medical Disclaimer.<\/strong> This page is for informational purposes only and does not replace medical advice from a qualified healthcare professional. Hypertension, heart failure, and arrhythmias require diagnosis, monitoring, and dose individualisation by a doctor &mdash; always use beta-blockers under medical guidance.<\/div>\n<p><!-- medsbase-related-alts-v1 --><\/p>\n<h3 class=\"wp-block-heading\">Related Alternatives<\/h3>\n<p>Other products in <strong>Chronic Conditions<\/strong> that customers also view:<\/p>\n<ul>\n<li><a href=\"https:\/\/medsbase.com\/endoxan\/\">Endoxan<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/glycomet-gp\/\">Glycomet-GP<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/trazonil\/\">Trazonil<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/cosart-h\/\">Cosart H<\/a><\/li>\n<li><a href=\"https:\/\/medsbase.com\/endace\/\">Endace<\/a><\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Dilvas is enalapril 2.5\/5\/10 mg tablets \u2014 ACE inhibitor first validated in the CONSENSUS trial (1987) which demonstrated 40% mortality reduction in severe heart failure, and SOLVD (1991) which extended the benefit to moderate HF. First-line for hypertension (particularly in patients under 55 and in diabetics), heart failure with reduced ejection fraction, post-MI LV dysfunction, and diabetic nephropathy. Take on an empty stomach. Dry cough (5-10%) is the most common class side effect.<\/p>\n","protected":false},"featured_media":51695,"comment_status":"open","ping_status":"open","template":"","meta":[],"product_brand":[],"product_cat":[3141,3223,3260,3356],"product_tag":[3395,3396],"class_list":{"0":"post-51694","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-category-overview","7":"product_cat-chronic-conditions","8":"product_cat-heart-blood-pressure","9":"product_cat-high-blood-pressure-medication","10":"product_tag-dilvas","11":"product_tag-elanapril","13":"first","14":"instock","15":"shipping-taxable","16":"purchasable","17":"product-type-variable","18":"has-default-attributes"},"acf":[],"_links":{"self":[{"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/product\/51694","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/comments?post=51694"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/media\/51695"}],"wp:attachment":[{"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/media?parent=51694"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/product_brand?post=51694"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/product_cat?post=51694"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/medsbase.com\/wp-json\/wp\/v2\/product_tag?post=51694"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}