Home
    Disclaimer
    Flunitrazepam molecular structure

    Flunitrazepam Stats & Data

    R2 Roches Roofies Ruffies Circles rohypnol
    Chemical Class Benzodiazepine
    Psychoactive Class Depressant
    Half-Life 18 – 26 hours (active metabolite norflunitrazepam contributes to tail)

    Pharmacology

    DrugBank
    Half-life 18-26 hours State Solid Metabolism Hepatic.

    Description

    Flunitrazepam is a benzodiazepine with pharmacologic actions similar to those of diazepam that can cause anterograde amnesia. Some reports indicate that it is used as a date rape drug and suggest that it may precipitate violent behavior. The United States Government has banned the importation of this drug.

    Mechanism of Action

    Benzodiazepines bind nonspecifically to benzodiazepine receptors BNZ1, which mediates sleep, and BNZ2, which affects affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABAA) receptors, this enhances the effects of GABA by increasing GABA affinity for the GABA receptor. Binding of the inhibitory neurotransmitter GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.

    Pharmacodynamics

    Flunitrazepam is a powerful hypnotic drug that is a benzodiazepine derivative. It has powerful hypnotic, sedative, anxiolytic, and skeletal muscle relaxant properties. The drug is sometimes used as a date rape drug. In the United States, the drug has not been approved by the Food and Drug Administration for medical use, and is considered to be an illegal drug. It has however been approved in the United Kingdom and other countries.

    Absorption

    50% (suppository) and 64-77% (oral)

    Toxicity

    Symptoms of overdose include confusion, coma, impaired coordination, sleepiness, and slowed reaction time.

    Indication

    For short-term treatment of severe insomnias, that are not responsive to other hypnotics.

    Receptor Profile

    Receptor Actions

    Modulators
    GABA-A receptor positive allosteric modulator (benzodiazepine site)

    Receptor Binding

    Translocator protein agonist

    History & Culture

    1960–1975

    Flunitrazepam was discovered at Hoffmann-La Roche as part of the benzodiazepine research program led by Leo Sternbach. The patent application was filed in 1960 and granted in 1962. Research during this period demonstrated that the specific molecular combination of an N-methyl group and 2-fluoro substitution produced particularly pronounced hypnotic effects compared to other benzodiazepine variants being investigated. The drug came into medical use in the early 1970s and entered the European commercial market in 1975 under the brand name Rohypnol. It was introduced as a treatment for severe insomnia and as a pre-anesthetic medication in hospital settings requiring deep sedation. Originally available in both 1 mg and 2 mg tablet formulations, it gradually expanded to additional international markets during the 1980s. The drug was never approved for medical use or marketed in the United States.

    1996–2016

    Growing concerns over recreational abuse and use in drug-facilitated crimes prompted the manufacturer Roche to implement several modifications throughout the 1990s. The 2 mg tablets were phased out between 1996 and 1999, and most European countries revised their regulations to limit the maximum available dose to 1 mg. In 1998, Roche introduced redesigned tablets intended to deter covert administration in beverages. The new formulation was made less soluble in cold liquids and incorporated a blue dye that would visibly color drinks when dissolved, while leaving green residue at the bottom of the container. These modifications were specifically designed to make detection easier in the cold beverages commonly served at social gatherings. By 2016, flunitrazepam had been withdrawn from commercial markets in Spain, France, Norway, Germany, and the United Kingdom. The drug remains available by prescription in some countries but faces significant regulatory restrictions across most jurisdictions.

    Flunitrazepam gained widespread notoriety during the 1990s as a "date rape drug," acquiring street names including "roofies" and "floonies." Its potent capacity to cause anterograde amnesia made it particularly alarming in the context of drug-facilitated sexual assault. However, harm reduction documentation notes that while this association became well-known in popular culture, such use represents a relatively small proportion of the drug's overall misuse patterns. In the United Kingdom, evidence suggests that flunitrazepam and similar sedatives have been more commonly connected to drug-assisted robbery than sexual assault, with activist estimates suggesting up to two thousand individuals may be robbed annually after consuming spiked drinks. Swedish epidemiological research found flunitrazepam to be the second most common drug detected in suicide cases, identified in approximately 16% of analyzed deaths. The substance has also circulated as a recreational sedative within rave and club scenes.

    Effect Profile

    Curated + 14 Reports
    Benzodiazepine 7.1

    Strong anxiolysis, cognitive impairment, and euphoria with mild sedation

    Anxiolysis×3
    10
    Sedation / Relaxation×2
    5
    Motor / Cognitive Impairment×1
    10
    Euphoria / Mood Lift×1
    10

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    18 – 26 hours (active metabolite norflunitrazepam contributes to tail)
    Addiction Potential
    High. Benzodiazepines carry substantial risks of tolerance, physiological dependence, and withdrawal; risk rises with daily use, high doses, or co-use of other CNS depressants.

    Tolerance Decay

    Full tolerance 21d Half tolerance 7d Baseline ~14d

    Clinical and community data indicate tolerance to hypnotic and anticonvulsant effects develops over weeks with regular use and decays over 1–4+ weeks after cessation; data are approximate and interindividual.

    Cross-Tolerances

    Other benzodiazepines
    80% ●○○
    Barbiturates
    30% ●○○
    Z-drugs (zolpidem/zopiclone)
    40% ●○○

    Experience Report Analysis

    Erowid
    14 Reports
    1993–2023 Date Range
    4 With Age Data
    5 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid

    Effects aggregated from 14 experience reports (14 Erowid)

    14 Reports
    5 Effects Detected
    4 Positive
    1 Adverse
    0 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 4

    Anxiety Suppression 57.1% 70%
    Sedation 50.0% 70%
    Stimulation 42.9% 70%
    Euphoria 42.9% 70%

    Adverse Effects 1

    Memory Suppression 28.6% 70%

    Real-World Dose Distribution

    62K Doses

    From 18 individual dose entries

    Oral (n=12)

    Median: 1.0mg 25th: 1.0mg 75th: 2.0mg 90th: 2.0mg
    mg/kg median: 0.016 mg/kg 75th: 0.024

    Form / Preparation

    Most common forms and preparations reported

    Benzodiazepine Equivalence

    1.0 mg Flunitrazepam = 10.0 mg Diazepam
    Potency ratio 10.0

    Flunitrazepam - 1mg ~=10mg Diazepam.

    Legal Status

    UN Convention on Psychotropic Substances 1971 (Schedule III)
    Country Status Notes
    Australia Schedule 8 Classified as a controlled drug requiring a valid prescription or license. Unauthorized possession may result in charges of trafficking in a drug of dependence. Only available in 1 mg tablets marketed under the brand name Hypnodorm.
    Austria Prescription required Legal for medical use under the Arzneimittelgesetz (AMG). Possession or sale without a valid prescription is prohibited under the Suchtmittelgesetz (SMG).
    Canada Schedule I CDSA Reclassified from Schedule III to Schedule I in 2012 under the Controlled Drugs and Substances Act. Production, distribution, and possession without authorization carry criminal penalties.
    Germany Anlage III BtMG Since November 2011, regulated under Anlage III of the Betäubungsmittelgesetz, requiring a special narcotic prescription form. Available in 1 mg tablets; 2 mg injectable ampoules are handled similarly to controlled narcotics like morphine.
    Netherlands Prescription medication Available by prescription in both 1 mg and 2 mg tablet formulations. Generic alternatives exist for the higher dosage form.
    Norway Controlled substance Classified as a controlled substance available only by prescription. Marketed under the brand name Flunipam.
    Sweden Class 2 Classified more strictly than most other benzodiazepines, which fall under Class 4. Available as a prescription medication in 0.5 mg and 1.0 mg tablet strengths.
    Switzerland Controlled narcotic Listed as a controlled narcotic substance. Occasionally prescribed as a sleep aid for severe insomnia. Tablets are dyed green and blue to deter covert administration in beverages.
    United Kingdom Class C, Schedule 4 Controlled under the Misuse of Drugs Act 1971 as a Class C substance and Schedule 4 under the Misuse of Drugs Regulations 2001. Approved for medical use and available by prescription.
    United States Schedule IV (federal); Schedule I (some states) Federally classified as Schedule IV under the Controlled Substances Act, but the FDA has not approved it for medical use, effectively making possession without a valid foreign prescription illegal. Importation is banned even for individuals holding valid prescriptions from other countries. Several states including Idaho, Minnesota, and Oklahoma have independently classified it as Schedule I, carrying stricter penalties.

    Harm Reduction

    drugs.wiki

    Harm-reduction essentials: (1) Potency and amnesia: flunitrazepam is a powerful hypnotic; small dose increments can cause profound sedation and anterograde amnesia, especially above ~1–2 mg. Avoid redosing during the first several hours because the peak may be delayed and effects accumulate with its long half-life. Evidence: HR organizations and pharmacology summaries report rapid onset, strong amnesia and long duration. (2) Mixing with depressants: combining benzodiazepines with alcohol, opioids, or GHB/GBL greatly increases the risk of respiratory depression, loss of consciousness, aspiration, and death. Treat these combinations as high-risk and avoid. If opioids may be present, keep naloxone accessible, but note that naloxone will not reverse benzodiazepine sedation. (3) Gabapentinoids and other sedatives: pregabalin/gabapentin and sedative-hypnotics (Z-drugs, antihistamines, carisoprodol) additively increase sedation and overdose risk; co-use features prominently in European overdose monitoring. (4) Grapefruit/CYP3A4: avoid grapefruit products and strong CYP3A4 inhibitors; they can raise flunitrazepam levels and prolong sedation. (5) Counterfeit risk and adulteration: tablets sold as “Rohypnol” on unregulated markets may contain other benzodiazepines or even potent synthetic opioids (e.g., nitazenes). Use trusted sources and, where available, drug checking to verify contents. (6) Overdose response: prioritize airway, breathing, and circulation; place an unconscious person in the recovery position and call emergency services. Flumazenil is not an at‑home antidote—it can precipitate dangerous seizures and withdrawal in benzodiazepine-tolerant individuals or mixed overdoses (e.g., with TCAs) and should only be considered in carefully selected medical settings. (7) Dependence and withdrawal: daily or prolonged use increases dependence risk; abrupt cessation after regular use can cause severe withdrawal and seizures. Any taper should be medically supervised; the FDA’s 2020 boxed warning for benzodiazepines underscores misuse, addiction, and withdrawal risks, especially with concurrent CNS depressants. (8) Next‑day impairment: due to an 18–26 h half-life and active metabolites, psychomotor impairment can persist into the next day—avoid driving or hazardous tasks until fully alert. (9) Sexual assault prevention and consent: never dose another person; be aware that flunitrazepam can cause hours of amnesia. Reduce victimization risk by not leaving drinks unattended, refusing unknown/open beverages, and looking out for peers. Seek immediate medical and legal assistance if drink‑tampering is suspected. (10) Populations at higher risk: older adults, people with respiratory disease or sleep apnea, and those on multiple sedatives are at heightened risk for respiratory events and falls; use extra caution or avoid.

    ← Back to Flunitrazepam