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Does selank ("Rita") actually cause anxiety? What the data says

judgetalkspeps

TikTok creator

1.3K viewsWatch on TikTok→

Quick answer

Retatrutide is an investigational GLP-1/GIP/glucagon triple receptor agonist currently in Phase 3 trials, with no FDA approval for any condition as of 2025. Its Phase 2 data (Jastreboff et al., NEJM 2023) documented significant weight loss efficacy but did not systematically evaluate psychiatric side effects including anxiety. Any compounded or gray-market retatrutide carries unknown purity and potency, making individual side effect reports difficult to interpret without knowing what compound was actually administered.

Our take · Written by FormBlends editorial team · Reviewed by FormBlends Medical Team· This is not a transcript. It is our independent review of the video above.

What did @judgetalkspeps actually say?

The creator says retatrutide (which they call "Retta") causes "really bad anxiety" for a viewer, but personally experiences the opposite: "it's like anti-anxiety for me." That's the whole claim. They're not citing a study or making a medical argument. They're crowdsourcing anecdotes in the comments, which is honestly a reasonable thing to do given how little clinical data exists on this peptide's psychiatric side effects.

To be clear about what this video is: it's two people comparing personal reactions to an investigational GLP-1/GIP/glucagon triple agonist that is not FDA-approved and is currently only in Phase 3 trials. The creator isn't prescribing anything or making therapeutic claims. They're sharing an experience and asking if others share it. That framing matters when evaluating what's actually being said.

Does the science back this up?

Sort of, but the data is thin and complicated. Anxiety as a side effect of GLP-1 receptor agonists has shown up in pharmacovigilance reports, but retatrutide specifically has almost no published psychiatric safety data.

The FDA's adverse event reporting system (FAERS) has flagged anxiety and related symptoms for GLP-1 class drugs more broadly. A 2023 analysis by Akbari et al. in Diabetes, Obesity and Metabolism noted neuropsychiatric signals in GLP-1 agonist users, though causality was not established. Retatrutide's Phase 2 trial published in NEJM (Jastreboff et al., 2023) reported nausea and GI events as primary side effects, with no specific mention of anxiety as a tracked outcome. That absence doesn't mean anxiety doesn't happen. It means the trials weren't designed to catch it.

The inverse reaction the creator describes, feeling calmer, is also biologically plausible. GLP-1 receptors are expressed in the amygdala and hippocampus, and some animal research suggests GLP-1 signaling may reduce stress responses. But "biologically plausible" is not the same as "proven in humans."

What did they get wrong (or right)?

They didn't get anything factually wrong, because they didn't make a factual claim. What they did was present two anecdotal reactions as if collecting them in comments will produce meaningful data. It won't. Self-reported anxiety on a peptide with no standardized dosing, no confirmed purity in compounded form, and no controlled conditions tells you almost nothing scientifically.

The creator deserves credit for one thing: they didn't claim their experience is universal or that the peptide is safe. The framing was genuinely open-ended. But the audience watching a TikTok about a non-FDA-approved compound may not automatically apply the same skepticism. Crowdsourcing side effect reports for an investigational drug sounds informal enough that people might interpret it as reassurance rather than genuine uncertainty.

The deeper issue is that "Retta" being used outside a clinical trial context means individual users have no idea what dose they're actually taking, what purity they have, or whether the compound is even retatrutide. That context was entirely missing from this video.

What should you actually know?

Retatrutide is not approved by the FDA for any indication as of 2025. It is an investigational triple agonist (GLP-1, GIP, glucagon receptors) being studied primarily for obesity. Any version being used outside a clinical trial is compounded or gray-market, with no verified purity or standardized dosing.

Psychiatric side effects of GLP-1 class drugs remain an open question. The FDA issued a 2023 safety communication acknowledging reports of suicidal ideation with semaglutide and liraglutide, though a causal relationship was not confirmed. Whether retatrutide carries similar signals is unknown, because the published trials did not systematically assess it.

Individual variation in anxiety response to any drug affecting central nervous system receptors is real and expected. Some people get anxious on beta-blockers. Some feel calmer on stimulants. Anecdote does not override the need for controlled data, and for retatrutide specifically, that data does not yet exist in the public domain for psychiatric outcomes.

If you are considering retatrutide and have a history of anxiety disorders, that is a conversation for a licensed clinician who can review your full history, not a TikTok comments section.

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This page currently connects to 7 source-backed evidence items through visible references or structured citation data.

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For Does selank ("Rita") actually cause anxiety? What the data says, FormBlends checks the page topic against primary trials, systematic reviews, guidelines, and current PubMed-indexed literature where available. These citations are context, not medical advice, proof of eligibility, or a claim that every study applies to every patient.

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Does selank ("Rita") actually cause anxiety? What the data says should be treated as a claim to verify, then compared with evidence, safety context, and a provider review path.

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Retatrutide is an investigational GLP-1/GIP/glucagon triple receptor agonist currently in Phase 3 trials, with no FDA approval for any condition as of 2025.

FormBlends verdict

Retatrutide is an investigational GLP-1/GIP/glucagon triple receptor agonist currently in Phase 3 trials, with no FDA approval for any condition as of 2025. Its Phase 2 data (Jastreboff et al., NEJM 2023) documented significant weight loss efficacy but did not systematically evaluate psychiatric side effects including anxiety. Any compounded or gray-market retatrutide carries unknown purity and potency, making individual side effect reports difficult to interpret without knowing what compound was actually administered.

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Use the clip as a claim to verify, not a treatment plan

What it helps with

  • Retatrutide is an investigational GLP-1/GIP/glucagon triple receptor agonist currently in Phase 3 trials, with no FDA approval for any condition as of 2025. Its Phase 2 data (Jastreboff et al., NEJM 2023) documented significant weight loss efficacy but did not systematically evaluate psychiatric side effects including anxiety. Any compounded or gray-market retatrutide carries unknown purity and potency, making individual side effect reports difficult to interpret without knowing what compound was actually administered.
  • Retatrutide has no FDA approval as of 2025. It is investigational, currently in Phase 3 trials for obesity treatment.
  • The NEJM Phase 2 trial (Jastreboff et al., 2023) did not systematically evaluate anxiety or other psychiatric outcomes as endpoints.

What it may miss

  • It may not cover eligibility, contraindications, medication interactions, lab history, or dose escalation.
  • Compound access, legal status, and product quality still need a separate safety check.
  • Social video captions rarely show the full evidence base behind a claim.

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What You'll Learn

  • Retatrutide has no FDA approval as of 2025. It is investigational, currently in Phase 3 trials for obesity treatment.
  • The NEJM Phase 2 trial (Jastreboff et al., 2023) did not systematically evaluate anxiety or other psychiatric outcomes as endpoints.
  • GLP-1 receptor agonists as a class have generated neuropsychiatric adverse event signals in FDA pharmacovigilance databases, but causal links have not been established.
  • GLP-1 receptors are present in the amygdala and hippocampus, making both pro-anxiety and anti-anxiety responses biologically possible in theory, but neither has been confirmed in human trials for retatrutide.
  • Compounded or gray-market retatrutide has no verified purity, potency, or identity, meaning side effect reports from users cannot be reliably attributed to the drug itself.
  • The FDA issued a 2023 safety communication about suicidal ideation signals with semaglutide and liraglutide. Whether retatrutide carries similar risks is not yet known from published data.
  • Anyone with a history of anxiety disorders considering any GLP-1 class compound should consult a licensed clinician before use, not base decisions on social media anecdotes.

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About the Creator

judgetalkspeps · TikTok creator

1.3K views on this video

Replying to @Littleraeofmoonshine #peptidepal does Rita make you anxious?

Sources & references

Citations extracted from our medical team's review. Click any citation to search PubMed.

Educational use only. This fact-check is editorial content for general information. Nothing here is medical advice. Talk to a licensed provider about your specific situation before starting, stopping, or changing any supplement, peptide, or medication regimen.

Read More on This Topic

Our written guides go deeper with dosing details, comparison tables, and medical-team reviewed protocols.

Not medical advice. This video was made by judgetalkspeps, not by FormBlends. Our write-up above is an editorial review, not a medical recommendation. Talk to your doctor before making any decisions about medications or treatments.