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ForumsCardiovascular OutcomesSemaglutide cardiovascular benefit independent of weight loss — looking for input Page 5

Semaglutide cardiovascular benefit independent of weight loss — looking for input

Dr.PeteFamMed Mon, Apr 27, 2026 at 1:38 AM 21 replies 664 viewsPage 5 of 5
VendorMark
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Apr 29, 2026 at 5:54 AM#21

From the other side of the consultation, briefly.

Dizziness and cardiovascular risk: I was lightheaded for the first 2 weeks. Root cause was a combination of reduced caloric intake and mild dehydration.

Fix: minimum 80-100oz water daily, don't skip meals even if you're not hungry (eat small protein-rich snacks), and stand up slowly from sitting/lying positions. Also check your blood pressure — GLP-1-induced weight loss can make BP meds too strong, requiring dose reduction.

Last edited: Apr 29, 2026 at 7:54 AM
3 3DebRD_ATL, KristenIndy, MarkLI_maint
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VanRx_Mike
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Apr 29, 2026 at 3:08 PM#22
VendorMark said:
Dizziness and cardiovascular risk: I was lightheaded for the first 2 weeks.

Adding a me-too, because a thread of one person's experience is not much use.

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Dr.GastroMayo
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Apr 30, 2026 at 12:22 AM#23
VendorMark said:
Dizziness and cardiovascular risk: I was lightheaded for the first 2 weeks.
VendorMark said:
...cardiovascular risk is just another fad...

I understand the skepticism — we've all seen "miracle" weight loss solutions come and go. But consider what makes GLP-1 agonists different:

  • Phase 3 RCTs with thousands of participants (not 20-person pilot studies)
  • Published in NEJM, JAMA, Lancet (not press releases)
  • Replicated across multiple independent research groups
  • Proven cardiovascular and renal benefits beyond weight loss
  • Biological mechanism fully characterized at the receptor level

This isn't a fad — it's a new drug class supported by the highest level of clinical evidence. The comparison to past fads is understandable but inappropriate.

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hank_denver
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Apr 30, 2026 at 9:36 AM#24

One concrete data point for the thread. For anyone assembling their own picture: Tmax is one to three days, terminal half-life about 165 to 170 hours, steady state at four to five weeks, and subcutaneous bioavailability near 89%. Those four numbers explain most of the questions people ask about timing.

Last edited: Apr 30, 2026 at 1:36 PM
50 0fiona_VT, denise_HTX, raj_cambridge and 47 others
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BariatricNurseD
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Apr 30, 2026 at 6:50 PM#25

A narrower follow-up, since the general answer is now clear:

What the dose-response curve actually looks like above 1.7mg, because the trial means hide how few people account for the extra loss?

Last edited: Apr 30, 2026 at 11:50 PM
49 24Dr.EndoIndy, tom_AK, josh_phd_bmore and 46 others
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