Saxenda side effects and stopping GLP-1s: what the data says
Quick answer
The creator and her partner discontinued liraglutide (Saxenda) after experiencing mood deterioration and heavy menstrual bleeding during weeks five to six of treatment. Huppy's pre-existing history of depression and anxiety is clinically relevant, as GLP-1 receptor agonist labels include warnings about monitoring for mood changes in patients with psychiatric history. Menstrual cycle disruption has been reported anecdotally with GLP-1 use, though the mechanism remains under investigation and may involve medication effects, hormonal shifts from weight loss, or both.
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 @fit2fat2fitagain actually say?
The creator says she and her partner "Huppy" both stopped taking Saxenda (liraglutide) after noticing significant mood changes. Huppy, who has a history of depression and anxiety since his teens, experienced mood declines around weeks five to six. She describes it as "a really, really rough time for a few weeks" before connecting it to the medication. She also reports two months of unusually heavy menstrual bleeding she'd never experienced before. Both stopped the medication about a month ago and report major wellbeing improvements.
She's careful to note this isn't universal: "This isn't for everybody, it's not going to affect everybody the exact same way." That caveat matters. This is a personal experience video, not a medical recommendation. But with 88K views, the framing carries weight whether she intends it to or not.
Does the science back this up?
On mood and depression, the evidence is genuinely complicated. There's no clean answer here, and anyone telling you otherwise hasn't read the literature carefully.
Liraglutide's prescribing information does list depression and suicidal ideation as potential risks requiring monitoring. The FDA added warnings about mood-related adverse events to GLP-1 receptor agonist labels after post-market surveillance flagged signals. A 2023 pharmacovigilance analysis by Rubino et al. in Nature Medicine reviewed WHO adverse event data and found that semaglutide was associated with lower rates of suicidal ideation compared to controls, which generated headlines. But liraglutide is a different molecule with different receptor binding profiles, and the same signal wasn't necessarily replicated across all GLP-1s. Pre-existing psychiatric history, as Huppy has, changes the risk calculus significantly.
On heavy menstrual bleeding, the evidence is thinner. There are case reports and emerging patient-reported data linking GLP-1 use to menstrual cycle changes, but no large randomized controlled trials have specifically isolated liraglutide as a cause of menorrhagia. The mechanism isn't well understood. Rapid weight loss itself can alter hormonal cycles, which complicates attribution.
What did they get wrong (or right)?
They got several things right. Flagging mood changes in someone with a documented psychiatric history as a possible medication side effect is clinically reasonable. The prescribing doctors were apparently informed of Huppy's depression and anxiety before starting, which is the correct process. Stopping a medication under medical supervision when adverse effects appear is also correct.
The heavy bleeding claim is trickier. She frames it as definitely Saxenda-related: "for the two months, it was just like unheard of." That's plausible, but it's also possible that weight changes, stress, or other factors were contributing. The honest answer is she can't know for certain, and neither can we without a controlled observation. She doesn't present it as confirmed, but the implied causation is stronger than the evidence supports.
What's missing is any mention of speaking to a gynecologist or getting hormonal panels checked. Menstrual disruption during weight loss intervention warrants investigation, not just medication cessation.
What should you actually know?
If you have a history of depression, anxiety, or other mood disorders, that's a conversation that needs to happen with your prescribing clinician before starting any GLP-1 medication, not after you notice a decline. The Saxenda label specifically recommends monitoring patients with a history of depression or suicidal ideation. That's not a theoretical warning.
GLP-1 receptors are expressed in the brain, including regions involved in mood regulation. Research is ongoing on whether this is therapeutically useful or a source of adverse effects in vulnerable individuals. A 2022 study by Mansur et al. in Journal of Affective Disorders explored GLP-1 agonists as potential mood modulators, but the bidirectional risk in people with existing psychiatric conditions is not resolved.
On the menstrual side, the FDA's Adverse Event Reporting System has received a growing number of reports about cycle disruption with GLP-1 use, but this hasn't translated into strong label warnings yet. If you experience significant menstrual changes on any GLP-1, report it to your doctor and ask about hormonal evaluation.
The creator's recommendation to stop if something doesn't feel right is reasonable advice in plain terms, but always do that in consultation with your prescriber, not unilaterally.
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For Saxenda side effects and stopping GLP-1s: 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.
Once-Weekly Semaglutide in Adults with Overweight or Obesity
Primary STEP 1 trial source for semaglutide weight-management efficacy and adverse-event context.
PubMed
Effect of Continued Weekly Subcutaneous Semaglutide vs Placebo on Weight Loss Maintenance
Used for maintenance, discontinuation, and weight-regain discussions after semaglutide response.
PubMed
Efficacy of GLP-1 Receptor Agonists on Weight Loss, BMI, and Waist Circumference
A broad meta-analysis anchor for GLP-1 weight-loss effect and class-level comparisons.
PubMed
Discontinuing glucagon-like peptide-1 receptor agonists and body habitus
Used for pages discussing stopping therapy, weight regain, and long-term planning.
PubMed
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The creator and her partner discontinued liraglutide (Saxenda) after experiencing mood deterioration and heavy menstrual bleeding during weeks five to six of treatment.
FormBlends verdict
The creator and her partner discontinued liraglutide (Saxenda) after experiencing mood deterioration and heavy menstrual bleeding during weeks five to six of treatment. Huppy's pre-existing history of depression and anxiety is clinically relevant, as GLP-1 receptor agonist labels include warnings about monitoring for mood changes in patients with psychiatric history. Menstrual cycle disruption has been reported anecdotally with GLP-1 use, though the mechanism remains under investigation and may involve medication effects, hormonal shifts from weight loss, or both.
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What it helps with
- The creator and her partner discontinued liraglutide (Saxenda) after experiencing mood deterioration and heavy menstrual bleeding during weeks five to six of treatment. Huppy's pre-existing history of depression and anxiety is clinically relevant, as GLP-1 receptor agonist labels include warnings about monitoring for mood changes in patients with psychiatric history. Menstrual cycle disruption has been reported anecdotally with GLP-1 use, though the mechanism remains under investigation and may involve medication effects, hormonal shifts from weight loss, or both.
- Saxenda's prescribing label explicitly lists depression and suicidal ideation as adverse events requiring patient monitoring, particularly in those with psychiatric history.
- A 2023 Rubino et al. Nature Medicine pharmacovigilance study found mixed mood-related signals across GLP-1 drugs, meaning results from one molecule like semaglutide do not automatically apply to liraglutide.
What it may miss
- It may not cover eligibility, contraindications, medication interactions, lab history, or dose escalation.
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- Social video captions rarely show the full evidence base behind a claim.
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Start provider reviewWhat You'll Learn
- Saxenda's prescribing label explicitly lists depression and suicidal ideation as adverse events requiring patient monitoring, particularly in those with psychiatric history.
- A 2023 Rubino et al. Nature Medicine pharmacovigilance study found mixed mood-related signals across GLP-1 drugs, meaning results from one molecule like semaglutide do not automatically apply to liraglutide.
- GLP-1 receptors are expressed in brain regions involved in mood and emotional regulation, but whether this causes benefit or harm in people with pre-existing depression is not yet resolved in clinical literature.
- Menstrual cycle disruption during GLP-1 treatment is increasingly reported in patient communities and to the FDA's FAERS database, but has not yet generated strong label-level warnings due to limited controlled trial data.
- Rapid weight loss from any intervention, not just GLP-1 medications, can independently disrupt menstrual cycles by altering estrogen and luteinizing hormone levels.
- Stopping a GLP-1 medication because of psychiatric adverse events is clinically reasonable, but should be done with your prescribing clinician involved, not unilaterally, to ensure proper monitoring and follow-up.
- Patients with a history of depression or anxiety starting any GLP-1 should discuss a mood monitoring plan with their prescriber before beginning treatment, not after symptoms appear.
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About the Creator
Fit2fat2fitagain · TikTok creator
88.3K views on this video
Why we stopped Saxenda! #saxendajourney #weightloss #saxenda
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 Fit2fat2fitagain, 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.