AOauto
AutoflowerModernTHC-Dominantevening

Auto Overdose

Top flavors

earthypinespicy
CalmingEnergizing

Auto Overdose effects are mostly calming.

Auto Overdose is a modern auto-flowering strain resulting from the cross of Afghani, Mexico Sativa, and Ruderalis genetics. The history and specific breeding origin of this variety remain undocumented, as no official breeder records identify the primary developer or the date of its creation. It is cultivated as an easy-to-grow plant that matures in 63 days of flowering, and it is suitable for both indoor and outdoor environments. Growers should note that the strain historically provides a low yield, reflecting its specific genetic expression.

The sensory profile of Auto Overdose is characterized by a complex array of terpenes, led by myrcene as the primary constituent. This profile continues with pinene, caryophyllene, and limonene, followed by beta-pinene, ocimene, and linalool. The composition is further rounded out by humulene, nerolidol, terpinolene, bisabolol, guaiol, and camphene. These compounds work in concert to define the strain's aromatic and flavor characteristics, though given the nature of botanical variance in modern auto-flowering varieties, the intensities of these individual constituents likely fluctuate based on specific cultivation conditions.

As a THC-dominant cultivar, Auto Overdose is associated with effects that are reported as relaxed, happy, and uplifted. These characteristics make it a functional selection for those seeking relief from stress and pain, or for users looking to manage sleep-related concerns. Currently, there are no recorded offspring attributed to this strain, leaving it as a singular entry in the modern genetic landscape.

Terpene Profile

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

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

earthy

●●●○

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

~28%

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.

~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

Autoflower

Photoperiod-independent. Flowers based on age, not light cycle. Compact and fast.

THC-Dominant

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

Genealogy

Parentage, ancestry, and genetic relatives of Auto Overdose.

Ancestry

Auto OverdoseFull tree →
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Composite Traits

Use caution if

daytime-productivitymorning-useevening-wind-down

Where to buy Auto Overdose

No verified dispensaries on file — find it on Leafly.

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What would Auto Overdose × ? 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 Auto Overdose

Similar strains

Same primary terpene with overlapping effects.

Frequently Asked Questions

Is Auto Overdose indica or sativa?

Auto Overdose is modeled here as a autoflower (photoperiod-independent).

What terpene is dominant in Auto Overdose?

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

Is Auto Overdose good for daytime use?

Auto Overdose 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.