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Somatropin (rhGH)

FDA ApprovedSince 1985
Also known as Genotropin, Norditropin, Humatrope, HGH

Get a source-linked, educational explanation from this profile.

Complete Research Guide

Open each section for the available evidence. Gaps are stated rather than inferred.

Overview

Somatropin (rhGH) is listed as gh axis / recombinant hormone.

  • •Growth hormone deficiency
  • •Short stature
  • •HIV wasting
  • •Off-label body composition / performance

Regulatory status: FDA-Approved Rx; non-medical use prohibited and WADA-banned.

Structure & Properties

Compound: Somatropin (rhGH); also known as Genotropin, Norditropin, Humatrope, HGH.

Pharmacologic class: GH Axis / Recombinant Hormone.

Known delivery routes: Subcutaneous, Intramuscular.

Sequence, molecular weight, salt form, and excipient details are formulation-specific and are not listed unless verified by a manufacturer or laboratory COA.

How It Works

Recombinant 191-amino-acid human growth hormone; binds GH receptor to drive hepatic IGF-1 output, lipolysis, and nitrogen retention.

  • •Increased lean mass and reduced visceral fat
  • •Improved recovery and connective tissue turnover
  • •Normalizes IGF-1 in true deficiency
Human Research

Evidence grade: Clinical RCT (Phase III)

Clinical RCT (Phase III). Extensively studied in GHD; performance use not approved.

Laboratory Research

Extensively studied in GHD; performance use not approved

Preclinical findings describe biological plausibility, not proven benefit in people. Animal and laboratory doses do not translate directly to human use.

Processing & Interactions

Timing and exposure

No strict time-of-day requirement. Dose consistently at the same time daily and rotate injection sites. Follow the per-peptide dosing section above.

Potential interactions and combinations to avoid

  • •Avoid stacking with peptides that share the same receptor or mechanism without clinical guidance.
  • •Avoid combining with alcohol or immunosuppressants unless cleared by a clinician.

Absorption, half-life, metabolism, and clearance can vary by formulation and route. Use prescribing information when an approved product exists.

Safety & Precautions

Known or reported risks

  • •Insulin resistance / hyperglycemia
  • •Carpal tunnel, edema, arthralgia
  • •Cardiac and organ hypertrophy with supraphysiologic use
  • •Possible tumor growth promotion

Contraindications

  • •Active malignancy
  • •Proliferative diabetic retinopathy
  • •Acute critical illness
  • •Closed epiphyses with non-approved indication
  • •Active malignancy or history of hormone-sensitive tumor (GH/IGF-1 axis stimulation)
  • •Active or untreated diabetic retinopathy
  • •Insulin resistance, prediabetes, or poorly controlled type 2 diabetes
  • •Untreated hypothyroidism or uncorrected adrenal insufficiency
  • •Acromegaly, pituitary adenoma, or intracranial hypertension
  • •Carpal tunnel syndrome, peripheral edema, or fluid-retentive heart failure
  • •Critical illness after acute surgery, trauma, or respiratory failure
  • •Severe obstructive sleep apnea (may worsen with soft-tissue growth)
  • •Bleeding disorders or anticoagulant therapy without physician guidance (injection-site haematoma)
  • •Active skin infection, cellulitis, or lipohypertrophy at intended injection sites
  • •Inability to maintain sterile technique or safe sharps disposal
  • •Prader-Willi syndrome with severe obesity or respiratory impairment
  • •Closed epiphyses when used for height indications
  • •Known hypersensitivity or prior reaction to this compound or any excipient/diluent
  • •Pregnancy, attempting conception, or breastfeeding unless prescribed and monitored by a physician
  • •Children and adolescents with open growth plates (unless under specialist endocrine care)
  • •Active or recently treated malignancy without oncology clearance
  • •Use without a confirmed diagnosis, baseline labs, and licensed clinical supervision

Unknown long-term toxicity should be assumed where controlled human data are limited. Seek urgent care for a severe or unexpected reaction.

Administration & Studied Formulations

Reference range: 0.15–0.6 mg/day (clinical); off-label performance use commonly 1–4 IU/day

Frequency: Daily, usually evening

Cycling: Clinical use is continuous with IGF-1 monitoring. Non-medical protocols often cycle 8–16 weeks, which does not remove metabolic risk.

Subcutaneous (SubQ)

Default route for most research and therapeutic peptides — best absorption for reconstituted powder.

31G × 5/16" insulin syringe (U-100). 100 units = 1 mL. Pinch skin at abdomen (2" from navel), outer thigh, or love handle. Insert at 45–90°. Rotate sites daily to prevent lipohypertrophy. Alcohol-swab site, air-dry, inject slow, hold 5 sec.

Intramuscular (IM)

Used for depot formulations, some GH secretagogues (localized delivery), and clinical protocols requiring faster systemic uptake.

23–25G × 1–1.5" needle. 1–3 mL syringe. Ventrogluteal, vastus lateralis, or deltoid. Insert 90°, aspirate (optional), inject slowly. Rotate sites weekly.

Dosing information is educational context, not a personal recommendation. Approved products must follow their label and prescriber instructions.

Applications & Related Therapies

Potentially complementary measures

  • •Most peptides pair safely with baseline nutrition, sleep, and resistance training.

Clinical use should account for diagnosis, approved alternatives, nutrition, activity, sleep, rehabilitation, current medicines, and appropriate monitoring.

Cases, Considerations & Ethics

Decision framework: establish the clinical goal, confirm evidence quality and legal status, screen contraindications and interactions, compare approved alternatives, define monitoring and stopping criteria, and use shared decision-making with a licensed clinician.

Case evidence: individual reports cannot establish safety or effectiveness and should not outweigh controlled trials.

Ethics: informed consent should distinguish established care from experimental use, disclose uncertainty and cost, avoid overstated claims, and never substitute research products for medically necessary care.

What is Somatropin (rhGH)?

In plain words

Somatropin is a lab-made version of human growth hormone. It signals the liver to make IGF-1 [a growth-promoting protein] and helps the body break down fat and retain nitrogen, a building block of proteins. It is studied and used medically for low growth hormone levels, short stature, and severe weight loss linked to HIV. Clinical trials support medical uses, but risks include high blood sugar, swelling, joint pain, and possible tumor growth; above-normal hormone levels can also enlarge the heart and other organs.

Technical definition

Somatropin (rhGH) is a recombinant human growth hormone consisting of 191 amino acids that binds the growth hormone receptor, stimulating hepatic IGF-1 production, lipolysis, and nitrogen retention. Phase III randomized controlled trial evidence supports its clinical use, with listed uses including growth hormone deficiency, short stature, and HIV wasting. It is an FDA-approved prescription drug; non-medical use is prohibited, and it is banned by WADA.

Function

Primary
Growth hormone deficiency · Short stature · HIV wasting
Secondary
Off-label body composition / performance
Mechanism
Recombinant 191-amino-acid human growth hormone; binds GH receptor to drive hepatic IGF-1 output, lipolysis, and nitrogen retention.
Evidence
Clinical RCT (Phase III)
Research
Extensively studied in GHD; performance use not approved

Dosing

Range
0.15–0.6 mg/day (clinical); off-label performance use commonly 1–4 IU/day
Frequency
Daily, usually evening
Route
Subcutaneous · Intramuscular

Recommended Time of Day

Before bed for anti-aging protocols; split morning/pre-bed at higher clinical doses.

See “Timing & Interactions” below for full fasted/fed circumstances, what to avoid combining, and what pairs well.

Administration & Technique

Subcutaneous (SubQ)
Default route for most research and therapeutic peptides — best absorption for reconstituted powder.
Device31G × 5/16" insulin syringe (U-100). 100 units = 1 mL.
TechniquePinch skin at abdomen (2" from navel), outer thigh, or love handle. Insert at 45–90°. Rotate sites daily to prevent lipohypertrophy. Alcohol-swab site, air-dry, inject slow, hold 5 sec.
Intramuscular (IM)
Used for depot formulations, some GH secretagogues (localized delivery), and clinical protocols requiring faster systemic uptake.
Device23–25G × 1–1.5" needle. 1–3 mL syringe.
TechniqueVentrogluteal, vastus lateralis, or deltoid. Insert 90°, aspirate (optional), inject slowly. Rotate sites weekly.

Injection & Application Sites

Front
Back
Subcutaneous (SubQ)
  • Abdomen — 2 in (5 cm) away from the navel, either side. Fastest, most consistent SubQ absorption.
  • Flank / love handle — Lateral fat pad above the hip. Good rotation site when the abdomen is tender.
  • Outer thigh — Upper outer quadrant, a hand-width below the hip. SubQ pinch at 45°.
Intramuscular (IM)
  • Ventrogluteal — Palm on greater trochanter, index to ASIS — inject in the V. Safest IM site.
  • Dorsogluteal (upper outer) — Upper outer quadrant of the buttock. Used for depot IM; alternate sides each cycle.
  • Upper arm / deltoid — Back of the upper arm for SubQ; 2 in below the shoulder bone for IM.
  • Anterior thigh (vastus lateralis) — Middle third of the outer front thigh. Preferred IM site for self-injection.

Diagram is a general illustration, not a medical instruction. Rotate sites every injection, keep 1 in (2.5 cm) between recent sites, and avoid scars, moles, bruises and the navel area.

Cycling

Clinical use is continuous with IGF-1 monitoring. Non-medical protocols often cycle 8–16 weeks, which does not remove metabolic risk.

Timing & Interactions

When to take
No strict time-of-day requirement. Dose consistently at the same time daily and rotate injection sites. Follow the per-peptide dosing section above.
Do not combine with
  • ·Avoid stacking with peptides that share the same receptor or mechanism without clinical guidance.
  • ·Avoid combining with alcohol or immunosuppressants unless cleared by a clinician.
Complements
  • ·Most peptides pair safely with baseline nutrition, sleep, and resistance training.

Storage & Reconstitution

Powder (Pre-Reconstitution)
Lyophilized powder: refrigerate 2–8°C for up to 24 months, or freeze at –20°C for extended storage. Keep sealed, desiccated, and protected from light.
After Reconstitution
After reconstitution with bacteriostatic water, refrigerate at 2–8°C and use within 28 days. Discard if cloudy, discolored, or precipitated.
Notes
Do not freeze after reconstitution — freeze/thaw cycles degrade most peptides.
Full BAC water & reconstitution guide →How to read a COA →

Reconstitution Calculator

Concentration
2.50 mg/mL
Volume per dose
0.100 mL
Insulin syringe
10.0 units (U-100)

1 mL = 100 units on a standard U-100 insulin syringe. Draw to the nearest 0.5 unit and confirm dosing with a clinician before injection.

Your Notes

Your Notes

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Benefits

  • ·Increased lean mass and reduced visceral fat
  • ·Improved recovery and connective tissue turnover
  • ·Normalizes IGF-1 in true deficiency

Risks

  • ·Insulin resistance / hyperglycemia
  • ·Carpal tunnel, edema, arthralgia
  • ·Cardiac and organ hypertrophy with supraphysiologic use
  • ·Possible tumor growth promotion

Contraindications

  • ·Active malignancy
  • ·Proliferative diabetic retinopathy
  • ·Acute critical illness
  • ·Closed epiphyses with non-approved indication
  • ·Active malignancy or history of hormone-sensitive tumor (GH/IGF-1 axis stimulation)
  • ·Active or untreated diabetic retinopathy
  • ·Insulin resistance, prediabetes, or poorly controlled type 2 diabetes
  • ·Untreated hypothyroidism or uncorrected adrenal insufficiency
  • ·Acromegaly, pituitary adenoma, or intracranial hypertension
  • ·Carpal tunnel syndrome, peripheral edema, or fluid-retentive heart failure
  • ·Critical illness after acute surgery, trauma, or respiratory failure
  • ·Severe obstructive sleep apnea (may worsen with soft-tissue growth)
  • ·Bleeding disorders or anticoagulant therapy without physician guidance (injection-site haematoma)
  • ·Active skin infection, cellulitis, or lipohypertrophy at intended injection sites
  • ·Inability to maintain sterile technique or safe sharps disposal
  • ·Prader-Willi syndrome with severe obesity or respiratory impairment
  • ·Closed epiphyses when used for height indications
  • ·Known hypersensitivity or prior reaction to this compound or any excipient/diluent
  • ·Pregnancy, attempting conception, or breastfeeding unless prescribed and monitored by a physician
  • ·Children and adolescents with open growth plates (unless under specialist endocrine care)
  • ·Active or recently treated malignancy without oncology clearance
  • ·Use without a confirmed diagnosis, baseline labs, and licensed clinical supervision

Regulatory

FDA-Approved Rx; non-medical use prohibited and WADA-banned

Veterinary Use (Pets)

No established veterinary protocol for Somatropin (rhGH). Consult a licensed veterinarian before considering off-label use in any species.

Full veterinary reference →
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Educational reference only. Not medical advice. Consult a qualified clinician before starting any peptide protocol.

Non-FDA-approved peptides are for research use only. Not for human or animal consumption.