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Healing & Recovery
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Tesamorelin
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Total Peptides: 32
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Healing & Recovery Protocol

Ziconotide (Prialt)Complete Dosing & Administration Guide

FDA-approved intrathecal analgesic derived from cone snail venom for severe chronic pain

Dose Range

2.4 mcg/day-19.2 mcg/daymcg

Frequency

Once daily

Route

Intrathecal infusion

Cycle Length

Ongoing/indefinite

Dosing

How much
do I take?

Timing

Best time to take

Use Ziconotide (Prialt) at the same time each day for optimal results. Consistency in timing helps maintain stable levels and maximize therapeutic benefits. Follow your healthcare provider's specific instructions.

With food?

Ziconotide (Prialt) can generally be used with or without food. If you experience any discomfort, try taking it with a light meal. Follow specific guidance from your healthcare provider.

If stacking

Ziconotide (Prialt) should be used as directed by your healthcare provider. If combining with other medications or supplements, discuss potential interactions with your provider. Avoid combining with compounds that have overlapping mechanisms unless specifically guided by a medical professional.

Adjusting Your Dose

Increase if

  • +You've tolerated the current dose for the recommended period without significant side effects
  • +Therapeutic goals haven't been met at the current dose level
  • +Your healthcare provider recommends dose escalation based on your response
  • +Lab work or clinical assessments support a higher dose

Decrease if

  • -Side effects are bothersome or impacting daily life despite management strategies
  • -You experience any signs of an adverse reaction
  • -Lab results indicate the need for dose reduction
  • -Your healthcare provider recommends a lower dose based on your response

Signs of right dose

  • Therapeutic goals being met with minimal side effects
  • Stable and consistent response to treatment
  • Lab values or clinical markers trending in the right direction
  • Good tolerance with manageable or absent side effects

Dosing Calculator

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Look for a number followed by 'mg' on the vial label (e.g., 5mg, 10mg)

Administration

How do I
use it?

Reconstitution

What you need

  • Ziconotide (Prialt) vial (lyophilized powder or solution)
  • Bacteriostatic water or sterile sodium chloride for reconstitution
  • Alcohol swabs for cleaning vial tops and injection sites
  • Appropriately sized syringes with fine-gauge needles (27-30 gauge)
  • Sharps disposal container

Example

Add the recommended volume of bacteriostatic water to the Ziconotide (Prialt) vial. Gently swirl (do not shake) until the powder is fully dissolved. The resulting solution should be clear. Calculate your individual dose based on the concentration and your prescribed amount.

Your dose of Ziconotide (Prialt) is determined by your healthcare provider. Using an insulin syringe marked in units, draw up the exact amount prescribed. For example, if the reconstituted concentration is 1mg/mL and your dose is 0.5mg, draw up 0.5mL (50 units on an insulin syringe). Always double-check calculations before injection.

Injection

Route

Subcutaneous injection (into the fatty tissue just under the skin)—allows for consistent absorption and can be self-administered at home after proper training

Best sites

  • Abdomen (stomach area)—at least 2 inches from the belly button, most popular choice for self-injection
  • Front of thighs—middle to upper portion of the outer leg
  • Back of upper arm—outer area (may need assistance from another person)

Technique

  • 1.Wash your hands thoroughly with soap and water before handling supplies
  • 2.Clean the injection site with an alcohol swab and let it air dry completely
  • 3.Pinch a fold of skin at the chosen injection site
  • 4.Insert the needle at a 45-90 degree angle (depending on needle length and body composition)
  • 5.Inject the medication slowly and steadily over 5-10 seconds
  • 6.Release the skin fold and remove the needle, applying gentle pressure with a clean swab
  • 7.Rotate injection sites to prevent tissue irritation or lipodystrophy
  • 8.Dispose of the needle safely in a sharps container—never recap or reuse needles

Storage

Before reconstitution

Store Ziconotide (Prialt) in the refrigerator at 36-46°F (2-8°C) in its original packaging. Protect from light and moisture. Do not freeze. Check the expiration date before use. Some formulations may be stored at room temperature for limited periods—check your specific product labeling.

After reconstitution

Once reconstituted, Ziconotide (Prialt) should be kept refrigerated at 36-46°F (2-8°C) and used within the timeframe specified on your product labeling (typically 14-28 days). Label the vial with the reconstitution date. Do not use if the solution appears cloudy, discolored, or contains particles.

Signs of degradation

  • Solution appears cloudy, discolored, or contains visible particles (should be clear)
  • Product has been exposed to temperatures outside the recommended storage range
  • Product has been frozen (unless specifically designed for freeze-thaw stability)
  • Expiration date has passed or reconstituted solution has exceeded its use-by date
  • Unusual odor, color change, or visible contamination

Sample Daily Schedule

As prescribed (once daily)

As prescribed by your healthcare provider injection

Site: Intrathecal infusion—rotate sites if applicable

Maintain a consistent schedule for optimal results with Ziconotide (Prialt). Set reminders if needed. If you miss a dose, follow your healthcare provider's instructions—do not double up on doses to compensate.

Safety

Is it
safe?

Safety Profile

Ziconotide (Prialt, FDA-approved since 2004) demonstrates favorable safety in intrathecal delivery with dose-dependent adverse effects primarily cognitive/psychiatric: dizziness, confusion, memory impairment, and mood changes in 20-50% of patients depending on infusion rate. Serious risks include meningitis-like aseptic meningitis (rare but documented), cognitive decline requiring dose reduction in ~25% of treated patients, and infection at intrathecal catheter insertion site. Hemodynamic effects (hypotension, dizziness) occur in dose-dependent fashion, necessitating slow titration (starting at 2.4 mcg/day, increasing weekly).

FDA approval based on Phase 2/3 trials in chronic pain patients demonstrating superior analgesia compared to placebo with manageable side effect profile when dosed carefully. Intrathecal route bypasses blood-brain barrier, achieving high spinal cord concentrations; safety monitoring must include cognitive/psychiatric assessment and CSF parameters. Over 15 years post-market experience supports acceptable benefit-risk profile in treatment-refractory cancer and non-cancer pain when dosed appropriately and infection risks minimized through proper catheter care.

Common Side Effects

Experienced by some users

Dizziness

Most common adverse effect reported in 46% of patients versus 13% placebo in clinical trials

Management: Usually manageable with dose adjustment; may improve with continued therapy

Nausea

Reported in 40% of patients; gastrointestinal effects also include diarrhea (18%) and vomiting (16%)

Management: Antiemetic medications as needed; often improves during dose stabilization

Less Common

  • Confusion and Memory Impairment
  • Ataxia and Nystagmus

These typically resolve with continued use or dose adjustment.

Stop and Seek Help If

  • ×Severe or worsening side effects that don't improve with dose adjustment or supportive care
  • ×Signs of an allergic reaction—rash, hives, swelling, or difficulty breathing
  • ×Your healthcare provider recommends discontinuation based on your clinical response
  • ×Development of any new medical condition that may be contraindicated with Ziconotide (Prialt)
  • ×Pregnancy or planning to become pregnant (unless specifically approved for use during pregnancy)
  • ×Abnormal lab results or clinical markers that suggest adverse effects

Ziconotide (Prialt) should only be started, adjusted, or discontinued under medical supervision. This information is for educational purposes only and does not replace professional medical advice. Never stop a prescribed treatment without consulting your healthcare provider first, as abrupt discontinuation may have consequences.

Interactions

With other peptides

  • Intrathecal baclofen may complement ziconotide for mixed pain and spasticity syndromes
  • Oral gabapentin addresses peripheral neuropathic pain through complementary calcium channel mechanisms
  • Rehabilitation combined with intrathecal analgesia optimizes functional recovery outcomes

With medications

  • !CNS Depressants - May potentiate central nervous system depression including somnolence and confusion
  • !Intrathecal Opioids - Concurrent intrathecal opioids increase risk of serious adverse events including respiratory depression
  • !Psychotropic Medications - May exacerbate psychiatric adverse effects including hallucinations and psychosis risk

With supplements

  • Multivitamins - Generally safe to take alongside Ziconotide (Prialt). Space doses apart if taking oral formulations to ensure optimal absorption.
  • Electrolyte supplements - Helpful if experiencing any GI side effects that could lead to dehydration. Safe to combine.

Want the Full Picture?

View the complete Ziconotide (Prialt) research profile including mechanism of action, clinical studies, effectiveness timeline, and FAQ.

View Full Ziconotide (Prialt) Profile

Medical Disclaimer

Ziconotide (Prialt) is an investigational research compound not approved by the FDA for human therapeutic use. This information is for educational purposes only and should not be construed as medical advice. Always consult with a qualified healthcare provider before starting any new supplement or treatment protocol.

Last updated: 2/8/2026