4 syllables: dom, per, i, done. Stress on per.
duhm-PUR-id-ohn
/dəmˈpɝɪdoʊn/
domperidone is pronounced duhm-PUR-id-ohn (/dəmˈpɝɪdoʊn/). It has four syllables (dom-per-i-done), with the stress on "per". Domperidone is a dopamine antagonist used to relieve nausea and gastroprokinetic symptoms. It works by blocking dopamine receptors in the gut and chemoreceptor trigger zones, promoting gut motility and reducing nausea signals. Typically administered orally or via suspension, its use requires medical supervision due to potential cardiac side effects and drug interactions.
Domperidone is a dopamine antagonist used to relieve nausea and gastroprokinetic symptoms. It works by blocking dopamine receptors in the gut and chemoreceptor trigger zones, promoting gut motility and reducing nausea signals. Typically administered orally or via suspension, its use requires medical supervision due to potential cardiac side effects and drug interactions.
- Common mistakes you’ll want to fix: 1) Misplacing stress on the second syllable or last syllable; practice dom-PER-i-done with a clear peak on PER. 2) Vowel reduction error in the second syllable; keep /ə/ or a quick schwa instead of a full /ʌ/ or /ɜ/. 3) Final sound mispronunciation: end with /doʊn/ or /dəʊn/ rather than /dɔn/; practice both, then pick the target accent. - How to correct: slow it to four syllables, incrementally speed up, finger-tap the rhythm, and record to check accuracy. - Practice steps: isolate the four syllables, tap each, then say at a normal pace, finally in a sentence.
"The patient was prescribed domperidone to alleviate persistent nausea."
"She took domperidone before the meal to improve gastric emptying."
"Doctors cautioned about QT prolongation risks when combining domperidone with other medications."
Pronounce as /ˌdɒmpəˈrɪdoʊn/ (US) or /ˌdɒmpəˈrɪdəʊn/ (UK/AU). Stress falls on the third syllable (ri) in doMPERiDONE; the sequence is dom-PER-i-done, with a light, schwa-like second syllable and a clear “ri” before the final “done.” Start with ‘doh’ plus mute ‘m’, then ‘puh’, then emphasize ‘ri,’ then finish with a soft ‘dohn’ or ‘deen’-like end depending on accent. An audio reference helps: listen for the crisp “ri” before the final diphthong.”,
Common errors: 1) Stressing the first or second syllable rather than the third (doM-PE-ri-done or dom-PE-ri-done). 2) Slurring or turning the final -done into a hard ‘done’ rather than a doh-n or deen ending; often heard as dom-pe-ri-dône. 3) Vowel quality errors in the second syllable; the unstressed second syllable should be a schwa /ə/ or a short /ə/; avoid an overly pronounced ‘uh’ or ‘ay.’ Corrections: rehearse dom-PER-i-done, keep the secondary stress on PER, and finish with either /doʊn/ or /doʊn/ depending on accent. Use minimal pairs to feel the rhythm.”,
In US English, you’ll hear /ˌdɒmpəˈrɪdoʊn/ with a U.S. rhotacized or non-rhotacized /ɒ/? Actually US ‘dɒm’ is /dɑm/ or /dɒm/. The primary stress remains on PER. UK and AU tend to /ˌdɒmpəˈrɪdəʊn/ with a longer final diphthong /əʊn/. The final -one may sound like 'ohn' or 'own' in US; in UK/AU it’s closer to /əʊn/. Vowel quality in the second syllable is generally a schwa in all; US may be slightly more relaxed; AU often shows a more rounded initial /ɒ/.”,
The difficulty stems from: 1) multi-syllabic length and a three-consonant cluster before the stressed syllable (domp-ER-i-done). 2) The mid syllable’s reduced vowel /ə/ can blur, making the word seem like two longer syllables. 3) Final -one can be realized as /oʊn/ or /ən/ depending on accent. You’ll hear quick speech in clinical settings; slow it down for accuracy, segment the word into four parts, and emphasize the ER syllable to stabilize rhythm.
A useful nuance is to perceive the word as four distinct syllables with a clear peak on the third syllable: dom-PER-i-done. Practically: say ‘dom’ (like 'dominate' without the ate), then a quick schwa, then a crisp /ɪ/ or /ɪ/ as in ‘rid,’ and finally a rounded ‘ohn’ or ‘deen’ ending. Keeping the middle syllable crisp while softening the final vowel helps mimic native medical pronunciation and reduces trailing off.
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US: /ˌdɒmpəˈrɪdoʊn/; non-rhotic or rhotic? US typically rhotics; UK/AU often non-rhotic in rapid speech but American rhotics are standard. Vowels: US /ɒ/ as in 'lot' for first syllable; UK/AU similar. The middle /ə/ is a schwa; the /ri/ is a clear ‘ri’ with a short vowel. The final /doʊn/ ends with a long diphthong in US, a more closed /dəʊn/ in UK/AU. Consonants: /d/ and /n/ are clear; no assimilation. - Try: emphasize the third syllable while keeping the final lightly pronounced to avoid adding an extra vowel. - IPA references: US /ˌdɒmpəˈrɪdoʊn/, UK/AU /ˌdɒmpəˈrɪdəʊn/.
Domperidone derives from a combination of roots in pharmaceutical naming conventions rather than a direct lineage from a single language. The stem ‘dom-’ echoes “domestic” or “domain” in early drug naming conventions, sometimes indicating target tissues or the direction of action, but in practice it’s a contrived sequence. The suffix ‘-peridone’ participates in a class of synthetic benzamide derivatives; the ‘-idone’ ending is common in pharmacological nomenclature for heterocyclic ring systems, borrowed from older medicinal chemistry nomenclature to denote a ring-containing compound with specific nitrogenous heterocycles. The name first appeared in scientific literature during late 20th-century drug development when dopamine antagonists for antiemetic and prokinetic properties were being characterized. Early pharmacologists serialized dozens of candidates; the official international nonproprietary name (INN) “domperidone” was standardized to reflect a distinctive chemical scaffold while hinting at its prokinetic activity. The word’s syllabic structure (dom-per-i-done) helps convey its multi-syllabic chemical identity, aiding memorability for clinicians and researchers. First known use in published pharmacology reports appears in the 1970s–1980s as researchers identified domperidone’s potency at gastrointestinal dopamine D2 receptors and noted its reduced central nervous system penetration relative to earlier agents. Over time, its clinical role expanded to include antiemetic use, with evolving cautions about cardiac safety that shaped regulatory labeling in different regions.
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