Research information only. Not medical advice. 18+ only. Not FDA-approved for human therapeutic use.

Felypressin

Also known as: PLV-2, Octapressin, 2-phenylalanine-8-lysine vasopressin, Felipressin

Synthetic vasopressin analogue / vasoconstrictor peptide

Research chemicalLast updated: October 10, 2026Based on 4 peer-reviewed studiesPreclinical data only — no human trials

What it is

Dentists use felypressin as a vasoconstrictor alongside prilocaine local anesthetic to reduce bleeding and prolong numbness during dental procedures. It is considered a safer epinephrine alternative for patients with cardiovascular conditions because it acts on vasopressin receptors rather than adrenergic receptors.

The scientific side

felypressin is a synthetic analogue of arginine vasopressin (AVP) that exerts its vasoconstricting effect primarily through vasopressin V1 receptor agonism rather than through adrenergic receptor stimulation. This receptor selectivity distinguishes it mechanistically from epinephrine (adrenaline), which acts on alpha- and beta-adrenergic receptors. Because felypressin does not stimulate adrenergic pathways, it avoids the tachycardia and increase in myocardial oxygen demand typically associated with epinephrine, making it a theoretically preferable vasoconstrictor in patients with certain cardiovascular comorbidities. When injected alongside a local anesthetic such as prilocaine, felypressin causes local vasoconstriction that slows systemic absorption of the anesthetic, prolongs the duration of anesthesia, reduces intraoperative bleeding, and limits peak plasma concentrations of the co-administered drug. Animal studies reported in the retrieved abstracts (Tachibana et al., PMID 34911066) showed that injection of 3% prilocaine with 0.03 IU felypressin transiently and significantly reduced pulpal blood flow (PBF) and pulpal oxygen tension (PpulpO2) in rabbits, with both measures recovering more rapidly than with lidocaine-epinephrine, suggesting a shorter duration of pulpal ischaemia with felypressin. Despite its non-adrenergic mechanism, felypressin is not without cardiovascular effect. A randomized controlled trial by Kyosaka et al. (PMID 31545671) found that prilocaine with felypressin increased both systolic and diastolic blood pressure in older adults, consistent with V1 receptor-mediated peripheral vasoconstriction. A separate study (Yamashita et al., PMID 31654643) demonstrated that prilocaine-felypressin increased sympathetic nervous activity during tooth extraction, in contrast to the parasympathetic suppression seen with lidocaine-epinephrine. Felypressin also carries oxytocic activity through its structural similarity to oxytocin: a 2025 systematic review (PMID 40649147) identified felypressin as contraindicated in pregnancy due to its capacity to stimulate uterine smooth muscle and induce contractions, which poses a risk to fetal wellbeing.

Class: Synthetic vasopressin analogue / vasoconstrictor peptide

Administration & storage

Administration
Buccal infiltration (supraperiosteal)Inferior alveolar nerve block (IANB)Intraligamentary (periodontal ligament) injectionInfiltration anesthesia under general anesthesia (intraoperative)
Storage
No specific storage data were reported in the retrieved abstracts. Standard pharmaceutical guidance for dental local anesthetic cartridges applies (protect from light, store at controlled room temperature, do not freeze).

Legal & regulatory status

US FDA

Not approved as a standalone dental vasoconstrictor in the United States; epinephrine-containing formulations are standard. Felypressin is not available in US dental cartridges.

WADA

Not listed on the WADA Prohibited List as of the abstracts reviewed; no doping-related data identified in the retrieved literature.

Health Canada

Available in Canada as a component of dental local anesthetic formulations (e.g., prilocaine with felypressin 0.03 IU/mL).