DVhybrid-indica
Hybrid-IndicaModernTHC-Dominantmorning

Deja vu

29%

THC

Top flavors

pineearthyspicy
CalmingEnergizing

Deja vu effects are mostly energizing.

Low THCHigh THC

Deja vu potency is higher THC than average.

Deja Vu is a modern hybrid-indica strain whose exact origins and development history remain undocumented by breeders. While its lineage is often associated with Chem 91 Skunk VA, there is no verified breeder description to confirm the specific cross or the intent behind its creation. Consequently, the development timeline and the identity of those responsible for bringing this strain to market remain subjects of speculation within the industry, as no formal cultivation records have been publicly established.

The terpene profile for Deja Vu is led by pinene, followed by myrcene, caryophyllene, limonene, ocimene, beta-pinene, humulene, linalool, bisabolol, guaiol, and nerolidol. Its cannabinoid content features an estimated 29% THC with approximately 0% CBD, though these figures are based on averaged data rather than batch-specific testing. Given this complex terpenoid array, the strain likely offers a multi-layered aromatic profile that transitions through the sharper, woody notes of pinene into the earthy, spicy, and floral undertones provided by its secondary and tertiary compounds.

Cultivators working with the strain note a flowering period of 63 days, with plants demonstrating enough resilience to thrive in both indoor and outdoor environments. Successfully managed, the strain produces an estimated high yield for growers of moderate experience. Clinically, Deja Vu is reported to deliver effects that are both relaxed and focused, making it a functional option for users managing pain, stress, or sleep-related concerns. There are currently no notable offspring recorded for this variety.

Terpene Profile

Synergies (+) and conflicts (−) are relative to each other within this profile.

pinene ~60%myrcene ~28%caryophyllene ~12%
TerpeneShare
pinene~60%
myrcene~28%
caryophyllene~12%

Research notes below describe isolated terpene mechanisms and early findings. They do not guarantee effects from this strain and are not medical advice.

~60%

pine

●●○○

Russo 2011: acetylcholinesterase inhibitor (IC50 0.44 mM) counteracting THC-induced short-term memory deficits; most widely encountered terpenoid in nature; anti-inflammatory via PGE-1.

~28%

earthy

●●●○

Russo 2011: naloxone-sensitive analgesia, potentiates barbiturate sleep; dominant sedating terpenoid; blocks hepatic carcinogenesis by aflatoxin.

~12%

spicy

●●○○

Russo 2011: only terpene that is a selective full CB2 agonist (100 nM); Gertsch et al. 2008: acts as dietary cannabinoid; unique anti-inflammatory and gastric cytoprotective properties.

Effects

Reported effects — derived from terpene chemistry and cannabinoid profile.

Genetic Profile

Indica-dominant

■ Indica 70%■ Sativa 30%

Primarily indica with sativa influence. Relaxing body with some cerebral lift.

THC-Dominant

High THC, trace CBD. Psychoactive. Full CB1 agonism — euphoria, appetite, analgesia.

Genealogy

Parentage, ancestry, and genetic relatives of Deja vu.

Composite Traits

Use caution if

evening-wind-downdaytime-productivitymorning-use

Where to buy Deja vu

No verified dispensaries on file — find it on Leafly.

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What would Deja vu × ? produce?

Predict the terpene profile, effects, and growing traits of a cross. Our gene weaver engine votes on dominant traits from both parents.

Build a cross with Deja vu

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Deja vu indica or sativa?

Deja vu is modeled here as a indica-dominant (primarily indica with sativa influence).

What terpene is dominant in Deja vu?

Pinene is shown as the dominant terpene at approximately ~60%. Myrcene follows as the secondary terpene.

Is Deja vu good for daytime use?

Deja vu is versatile and works across different times of day depending on dose and individual response.

How accurate is this data?

See the "Data confidence" card in the sidebar. Terpene profiles and effects are chemistry-informed estimates — individual responses depend on phenotype, source, and personal chemistry.