FDA Drug Label
GEREF (sermorelin acetate) for injection - Prescribing Information
Serono, 1997
GHRH 1-29
Sermorelin acetate (GHRH 1-29) is a synthetic analog of the first 29 amino acids of endogenous growth hormone-releasing hormone. FDA-approved for diagnosing and treating GH deficiency, it stimulates the pituitary gland to produce and secrete growth hormone naturally — a preferred alternative to exogenous HGH therapy for physiological GH optimization. Available by prescription through compounding pharmacies and telehealth providers.
Overall check-ins
Trackers & reports
Overview
Sermorelin acetate (GHRH 1-29) is a synthetic analog of the first 29 amino acids of endogenous growth hormone-releasing hormone. FDA-approved for diagnosing and treating GH deficiency, it stimulates the pituitary gland to produce and secrete growth hormone naturally — a preferred alternative to exogenous HGH therapy for physiological GH optimization. Available by prescription through compounding pharmacies and telehealth providers.
Community
From check-in ratings — separate from side effects logged below. Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.
Favorable 90% · Mixed 10% · Unfavorable overall 0%
Benefits users selected when logging a favorable or mixed check-in.
Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.
Median bucket: 0.2–0.4 mg · Most common: 0.2–0.4 mg
Reports span 0.2 to ≥ 5 mg (open-ended top bucket)
Anonymized self-reports from PeptIQ users — not prescribing guidance. Buckets group similar logged amounts; open-ended top buckets mean “at least” that dose.
Among repeat reporters, 81% said they felt similar to their last entry, 8% more positive, and 12% more negative.
Overall, repeat reporters leaned more negative than their previous entry.
Median gap between entries: 105 days · Based on 26 repeat reporters
Research
FDA Drug Label
Serono, 1997
PubMed
Ghigo et al., 2008
ClinicalTrials.gov
ClinicalTrials.gov, 2024
PubMed
Grossman et al., 1986
Tools
More ways to learn about Sermorelin from observational PeptIQ data.
Compare with
Related peptides
Help
This page summarizes 36 anonymized self-reports from PeptIQ users who track Sermorelin, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.
PeptIQ separates overall check-in ratings (favorable, mixed, or unfavorable) from logged side effects like nausea or fatigue. Users often report benefits and side effects in the same check-in — a high experience score does not mean zero side effects were noted.
4 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.
This wiki does not assess safety or recommend use. Sermorelin is listed as FDA Approved. Consult a licensed clinician for personal medical decisions.
This wiki summarizes observational community reports and linked citations for Sermorelin. It does not assert therapeutic benefits. See the cited research list on this page and the educational profile for Sermorelin for study-level context — not medical advice.
Sermorelin is listed in PeptIQ as FDA Approved. Regulatory status varies by jurisdiction and can change. This wiki does not provide legal advice; check current FDA and local rules and talk with a licensed clinician or counsel for personal decisions.
Safety data quality for Sermorelin varies widely by compound and study design. PeptIQ does not establish a risk profile here. Review primary literature, product labeling where applicable, and clinician guidance. Community self-reports are not a substitute for clinical evidence.
This page links 4 indexed sources for Sermorelin. Evidence maturity differs by application — some peptides have large human programs, others are mostly preclinical. Treat citation counts as literature volume, not proof of efficacy.