
Flunitrazepam, marketed under the brand name Rohypnol by Roche, is a potent intermediate-to-long-acting nitrobenzodiazepine approximately 10 times more potent than diazepam. It produces pronounced sedation, anxiolysis, anterograde amnesia, and muscle relaxation, and has legitimate pharmaceutical applications in anesthesia and the short-term treatment of severe insomnia in countries where it is licensed. In the United States, flunitrazepam has never been approved for medical use and is classified as a Schedule IV controlled substance (despite being unapproved), reflecting its high abuse potential and association with drug-facilitated sexual assault — a designation that makes its importation a federal offense.
Flunitrazepam became notorious in the United States and elsewhere from the early 1990s onward as a "date rape drug," primarily because its combination of profound sedation, anterograde amnesia, and (in older formulations) water solubility made it suitable for covert administration in beverages. Roche responded to this concern in the mid-1990s by reformulating the tablet to contain a blue dye that discolors clear liquids and makes the tablet harder to dissolve invisibly. However, generic and counterfeit versions may not contain these safety features.
The term "roofies" has become a generic colloquialism for drug-facilitated sexual assault drugs generally, though the actual prevalence of flunitrazepam specifically relative to other drugs (including alcohol) in such assaults has been contested by toxicological evidence. From a pharmacological harm reduction perspective, flunitrazepam's profile — high potency, pronounced amnesia, respiratory depression potential, and severe dependence/withdrawal risk — is shared by several other benzodiazepines; its cultural notoriety does not make it uniquely dangerous among the class, though its specific association with assault warrants clear harm reduction messaging.
Safety at a Glance
High Risk- Awareness of Context of Use
- Do Not Accept Open Drinks
- Toxicity: Anterograde Amnesia Flunitrazepam's most clinically concerning property is its pronounced anterograde amnesia, which ...
- Dangerous with: 1,4-Butanediol, 2M2B, Acetylfentanyl, Alcohol (+59 more)
- Overdose risk: overdose is a medical emergency that may lead to a coma, permanent brain injury or death if not t...
If someone is in crisis, call 911 or Poison Control: 1-800-222-1222
Dosage
oral
Duration
oral
Total: 4 hrs – 8 hrsHow It Feels
Flunitrazepam commands attention from the moment of onset. Within fifteen to twenty minutes, a heavy, warm sedation rolls through the body with the unstoppable momentum of a slow avalanche. The muscles relax deeply and completely, as though every fiber had simultaneously decided to stop holding tension. There is an immediate and dramatic reduction in anxiety -- not the gentle dimming of worry that milder benzodiazepines provide, but a wholesale deletion of the anxious substrate, leaving behind a calm so profound it borders on emptiness.
The come-up intensifies the sedation and introduces a hypnotic quality that distinguishes this substance from its less potent relatives. The eyelids become heavy with an almost magnetic pull, and the visual world softens and blurs at the edges. Thoughts slow to a crawl, each one arriving as though wading through warm honey. There is a euphoria -- muted but real -- that manifests as a deep, physical contentment, a feeling that the body has finally found the position it was always meant to be in and will not be moving from it anytime soon. Speech becomes thick and imprecise, and the motivation to communicate diminishes in proportion to the growing desire to simply exist in the warm darkness behind closed eyes.
At the peak, the hypnotic and amnestic properties dominate. Memory recording becomes unreliable, and the continuous thread of experience begins to fray and snap. Moments exist in isolation, disconnected from what came before or after, like islands in a dark sea. The sedation is so heavy that consciousness itself feels like a luxury being slowly revoked. The body is warm, heavy, and utterly still. The world at the peak of flunitrazepam is a small, dark, comfortable room from which you cannot remember entering and will not remember leaving.
The offset is a long, slow emergence from pharmacological twilight. Sleep -- deep, dreamless, and prolonged -- is almost inevitable. Waking brings a thick grogginess that can persist for hours, and the amnestic gaps may be substantial, whole stretches of time simply unaccounted for. The residual muscle relaxation can last well into the following day, and there is often a lingering sense of detachment from the world, as though consciousness has not yet fully recommitted to the business of being awake.
Subjective Effects
The effects listed below are based on the Subjective Effect Index (SEI), an open research literature based on anecdotal reports and personal analyses. They should be viewed with a healthy degree of skepticism. These effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects.
Physical Effects
Physical(14)
- Decreased blood pressure— Decreased blood pressure (hypotension) is a drop in arterial blood pressure below normal levels, com...
- Decreased heart rate— Decreased heart rate (bradycardia) is a slowing of the heart's rhythm below the normal resting range...
- Dizziness— A sensation of spinning, swaying, or lightheadedness that impairs balance and spatial orientation, o...
- Dry mouth— A persistent, uncomfortable reduction in saliva production causing the mouth and throat to feel parc...
- Insomnia— A persistent inability to fall asleep or maintain sleep despite physical tiredness, often characteri...
- Motor control loss— A distinct decrease in the ability to control one's physical body with precision, balance, and coord...
- Muscle relaxation— The experience of muscles throughout the body losing their rigidity and tension, becoming noticeably...
- Nausea— An uncomfortable sensation of queasiness and stomach discomfort that may or may not lead to vomiting...
- Perception of bodily heaviness— Perception of bodily heaviness is the subjective feeling that one's body has become dramatically hea...
- Physical euphoria— An intensely pleasurable bodily sensation that can manifest as waves of warmth, tingling electricity...
- Respiratory depression— A dangerous slowing and shallowing of breathing that can progress from barely noticeable reductions ...
- Sedation— A state of deep physical and mental calming that manifests as a progressive desire to remain still, ...
- Seizure— Uncontrolled brain electrical activity causing convulsions and loss of consciousness -- a life-threa...
- Seizure suppression— Seizure suppression is the pharmacological reduction or prevention of seizures through substances th...
Cognitive & Perceptual Effects
Cognitive(20)
- Amnesia— A complete or partial inability to form new memories or recall existing ones during and after substa...
- Analysis suppression— Analysis suppression is a cognitive impairment in which the capacity for logical reasoning, critical...
- Anxiety— Intense feelings of apprehension, worry, and dread that can range from a subtle background unease to...
- Anxiety suppression— A partial to complete suppression of anxiety and general unease, producing a calm, relaxed mental st...
- Cognitive euphoria— A cognitive and emotional state of intense well-being, elation, happiness, and joy that manifests as...
- Compulsive redosing— An overwhelming, difficult-to-resist urge to continuously take more of a substance in order to maint...
- Confusion— An impairment of abstract thinking marked by a persistent inability to grasp or comprehend concepts ...
- Delusion— A delusion is a fixed, false belief that is held with unshakeable certainty and is impervious to con...
- Depression— A persistent state of low mood, emotional numbness, hopelessness, and diminished interest or pleasur...
- Disinhibition— A marked reduction in social inhibitions, self-consciousness, and behavioral restraint that manifest...
- Dream potentiation— Enhanced dream vividness, complexity, and recall, often occurring as REM rebound after discontinuing...
- Dream suppression— Dream suppression is a decrease in the intensity, frequency, and recollection of dreams — ranging fr...
- Emotion suppression— A blunting or flattening of emotional experience in which feelings become muted, distant, or seeming...
- Irritability— Irritability is a sustained state of emotional reactivity in which the threshold for annoyance, frus...
- Language suppression— A diminished ability to formulate, comprehend, or articulate language, ranging from difficulty findi...
- Memory suppression— A dose-dependent inhibition of one's ability to access and utilize short-term and long-term memory, ...
- Motivation suppression— Motivation suppression is a state of diminished drive and willingness to engage in goal-directed beh...
- Sleepiness— A progressive onset of drowsiness, heaviness, and the desire to sleep that pulls the individual towa...
- Thought deceleration— The experience of thoughts occurring at a markedly reduced pace, as if the mind has been placed into...
- Thought disorganization— Thought disorganization is a cognitive impairment in which the normal capacity for structured, seque...
Pharmacology
Mechanism of Action
Flunitrazepam is a positive allosteric modulator of GABA-A receptors, binding to the benzodiazepine site and potentiating GABA-mediated chloride conductance. A nitro group (-NO2) at the 7-position of the benzene ring and a fluorine atom at the 2' position of the phenyl ring distinguish it structurally from diazepam. The nitro group enhances receptor binding affinity, contributing to the approximately 10-fold greater potency versus diazepam.
Pharmacokinetics
- Bioavailability: ~80% oral
- Onset: 15–30 minutes oral
- Half-life: 18–26 hours
- Active metabolites: N-desmethylflunitrazepam and other hydroxylated metabolites (active, extending pharmacological duration)
- Duration of effects: 4–8 hours clinically; residual impairment longer
The combination of the parent compound's moderate half-life and active metabolites produces a total pharmacological duration longer than the subjective effect duration — a pattern common to many benzodiazepines that contributes to day-after impairment.
Amnesia
Flunitrazepam produces pronounced anterograde amnesia at recreational and supratherapeutic doses, disproportionate to the degree of sedation. This property is associated with α1-GABA-A receptor subunit engagement and is characteristic of the nitrobenzodiazepine class. The amnesia can begin at doses that do not produce unconsciousness, meaning a person may appear awake and interact normally while forming no memories of events.
Potency
At approximately 10x diazepam potency, flunitrazepam is active at doses of 0.5–2 mg therapeutically. This high potency, combined with the amnestic profile, is the pharmacological basis for its misuse in drug-facilitated assault.
Detection Methods
Standard Drug Panel Inclusion
Flunitrazepam (Rohypnol) is detected on standard 10-panel drug screens and extended benzodiazepine panels, though its detection has historically been inconsistent. Older immunoassay platforms had poor cross-reactivity with 7-aminoflunitrazepam, the primary metabolite. In response to concerns about drug-facilitated sexual assault, manufacturers reformulated their assays to improve flunitrazepam detection, and current-generation immunoassays detect it with much greater reliability.
Urine Detection
Flunitrazepam and its metabolite 7-aminoflunitrazepam are detectable in urine for approximately 3 to 5 days after a single dose, with chronic users potentially testing positive for up to 2 weeks. The metabolite 7-aminoflunitrazepam is the primary target for both screening and confirmation. At therapeutic doses of 1 to 2 mg, urine concentrations may be low enough to approach the cutoff threshold of standard immunoassays, making hydrolysis and sensitive analytical methods important for reliable detection. In forensic cases involving suspected drug-facilitated crimes, laboratories often use lower cutoff values.
Blood and Serum Detection
Blood detection windows are 12 to 48 hours after ingestion. Therapeutic concentrations range from 5 to 15 ng/mL. Because flunitrazepam is active at very low doses, blood concentrations in assault cases may be extremely low, requiring analytical methods with sub-nanogram sensitivity.
Hair Follicle Detection
Hair analysis can detect flunitrazepam for up to 90 days and is particularly valuable in drug-facilitated assault investigations where delayed reporting makes urine testing impractical. Both flunitrazepam and 7-aminoflunitrazepam are targeted, with LC-MS/MS methods achieving limits of detection at 0.5 to 1 pg/mg of hair.
Confirmatory Methods
LC-MS/MS is the definitive confirmatory method for flunitrazepam, achieving limits of detection below 1 ng/mL in urine and below 0.5 ng/mL in blood. GC-MS with negative chemical ionization is an alternative that provides excellent sensitivity for this compound. Forensic laboratories typically use dedicated methods optimized for flunitrazepam given its significance in assault cases.
Reagent Testing
The Zimmermann reagent produces a yellow-green response with flunitrazepam. Mandelin yields an orange-brown color. These tests cannot distinguish it from other nitrobenzodiazepines. Immunoassay-based drink testing kits have been developed specifically to detect flunitrazepam in beverages, though their reliability varies.
Interactions
| Substance | Status | Note |
|---|---|---|
| 1,4-Butanediol | Dangerous | Combined CNS depression; risk of respiratory failure |
| 2M2B | Dangerous | Combined CNS depression; risk of respiratory failure |
| Acetylfentanyl | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Alcohol | Dangerous | Combined CNS depression; risk of respiratory failure |
| Alprazolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Atropa belladonna | Dangerous | Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure |
| Baclofen | Dangerous | Combined CNS depression; risk of respiratory failure |
| Benzodiazepines | Dangerous | Combined CNS depression; risk of respiratory failure |
| Buprenorphine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Cake | Dangerous | Combined CNS depression; risk of respiratory failure |
| Carisoprodol | Dangerous | Combined CNS depression; risk of respiratory failure |
| Clonazepam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Clonazolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Clonidine | Dangerous | Combined CNS depression; risk of respiratory failure |
| Codeine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Datura | Dangerous | Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure |
| Deschloroetizolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Desomorphine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Dextropropoxyphene | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Diazepam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Diclazepam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Dihydrocodeine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Diphenhydramine | Dangerous | Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure |
| Eszopiclone | Dangerous | Combined CNS depression; risk of respiratory failure |
| Ethylmorphine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Etizolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| F-Phenibut | Dangerous | Combined CNS depression; risk of respiratory failure |
| Fentanyl | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Flualprazolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Flubromazepam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Flubromazolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Flunitrazolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Gabapentin | Dangerous | Combined CNS depression; risk of respiratory failure |
| Gaboxadol | Dangerous | Combined CNS depression; risk of respiratory failure |
| GBL | Dangerous | Combined CNS depression; risk of respiratory failure |
| GHB | Dangerous | Combined CNS depression; risk of respiratory failure |
| Grayanotoxin | Dangerous | Combined CNS depression; risk of respiratory failure |
| Harmala alkaloid | Dangerous | Unpredictable potentiation of CNS depression; risk of respiratory failure |
| Heroin | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Hydrocodone | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Hydromorphone | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Kratom | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Lorazepam | Dangerous | Combined CNS depression; risk of respiratory failure |
| MAOI | Dangerous | Unpredictable potentiation of CNS depression; risk of respiratory failure |
| Mephenaqualone | Dangerous | Combined CNS depression; risk of respiratory failure |
| Methadone | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Methaqualone | Dangerous | Combined CNS depression; risk of respiratory failure |
| Metizolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Midazolam | Dangerous | Combined CNS depression; risk of respiratory failure |
| Mirtazapine | Dangerous | Combined CNS depression; risk of respiratory failure |
| Morphine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Myristicin | Dangerous | Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure |
| Naloxone | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Nicotine | Dangerous | Combined CNS depression; risk of respiratory failure |
| Nifoxipam | Dangerous | Combined CNS depression; risk of respiratory failure |
| O-Desmethyltramadol | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Oxycodone | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Oxymorphone | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Peganum harmala | Dangerous | Unpredictable potentiation of CNS depression; risk of respiratory failure |
| Pentobarbital | Dangerous | Combined CNS depression; risk of respiratory failure |
| Pethidine | Dangerous | Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths |
| Phenobarbital | Dangerous | Combined CNS depression; risk of respiratory failure |
| SAMe | Dangerous | Combined CNS depression; risk of respiratory failure |
| 2-Aminoindane | Caution | Masks the effects of each drug; risk of overdosing when one wears off before the other |
| 2-FA | Caution | Masks the effects of each drug; risk of overdosing when one wears off before the other |
| 2-FEA | Caution | Masks the effects of each drug; risk of overdosing when one wears off before the other |
| 2-Fluorodeschloroketamine | Caution | Both cause CNS depression; increased risk of vomiting, unconsciousness, and respiratory depression |
| 2-FMA | Caution | Masks the effects of each drug; risk of overdosing when one wears off before the other |
| 1,3-Butanediol | Low Risk & Decrease | Depressants dull psychedelic effects; benzodiazepines are commonly used as trip-killers |
| 1B-LSD | Low Risk & Decrease | Depressants dull psychedelic effects; benzodiazepines are commonly used as trip-killers |
| 1cP-AL-LAD | Low Risk & Decrease | Depressants dull psychedelic effects; benzodiazepines are commonly used as trip-killers |
| 1cP-LSD | Low Risk & Decrease | Depressants dull psychedelic effects; benzodiazepines are commonly used as trip-killers |
| 1cP-MiPLA | Low Risk & Decrease | Depressants dull psychedelic effects; benzodiazepines are commonly used as trip-killers |
History
Pharmaceutical Development
Flunitrazepam was developed by Roche and first marketed as Rohypnol in Europe and Latin America in the 1970s for use as a sedative-hypnotic. It was used in clinical anesthesia practice and for severe insomnia, representing a relatively mainstream pharmaceutical product in countries where it was approved. It was never approved in the United States or Canada, though it was available through importation.
Association with Drug-Facilitated Sexual Assault
Reports of flunitrazepam being used to facilitate sexual assault emerged significantly in the early-to-mid 1990s, particularly in US college communities. In 1996, the US Congress passed the Drug-Induced Rape Prevention and Punishment Act, establishing enhanced federal penalties for use of any controlled substance to facilitate violence. In the same period, media coverage of "Rohypnol" or "roofies" created widespread awareness of its misuse.
Reformulation Response
Roche reformulated Rohypnol in 1997 to contain a blue dye (FD&C Blue No. 1) that visibly colors clear beverages when dissolved, and changed the tablet to be harder to grind and dissolve. Generic versions marketed elsewhere may not contain these safety modifications.
Contemporary Regulatory Status
Flunitrazepam is Schedule IV in the United States (unusual given lack of FDA approval) and varies in scheduling across other jurisdictions. It remains a licensed pharmaceutical in several European, Latin American, and Asian countries. Its availability on illicit markets persists, often as diverted pharmaceutical product from countries where it remains legally manufactured.
Harm Reduction
Awareness of Context of Use
For individuals receiving or consuming substances in social settings: flunitrazepam and other sedating drugs can be covertly administered. Symptoms of covert drugging include sudden unexpected sedation, impaired speech and motor control, confusion, and memory gaps. If you or a friend experience these symptoms unexpectedly, move to a safe location and call for medical assistance.
Do Not Accept Open Drinks
Basic harm reduction for drug-facilitated assault situations: do not accept drinks you did not see poured from unopened containers, do not leave drinks unattended, and do not consume a drink that tastes unusual or bitter.
Standard Benzodiazepine Safety Applies
For those using flunitrazepam in other contexts: all standard benzodiazepine harm reduction applies — no combination with alcohol or opioids, accurate low-dose titration, avoidance of regular use, and gradual taper if dependence has developed.
Drug Testing
Drug testing strips for benzodiazepines can detect flunitrazepam in beverages. Fentanyl test strips are available separately. Both can be useful harm reduction tools in party or social settings.
Seek Medical Attention for Overdose
Suspected flunitrazepam overdose — profound sedation, respiratory depression, or unresponsiveness — warrants emergency medical attention. Flumazenil, the benzodiazepine antagonist, can reverse effects but has short duration and may require repeated dosing.
Toxicity & Safety
Anterograde Amnesia
Flunitrazepam's most clinically concerning property is its pronounced anterograde amnesia, which occurs at doses that do not necessarily produce unconsciousness. Individuals under flunitrazepam's influence may appear awake and coherent while subsequently having no memory of events. This combination underlies the drug's misuse in the context of sexual assault.
Respiratory Depression
Like all benzodiazepines, flunitrazepam produces dose-dependent respiratory depression, with synergistic risk when combined with alcohol or opioids. Its higher potency relative to diazepam means that smaller absolute doses can produce clinically significant respiratory depression.
Physical Dependence and Withdrawal
Regular flunitrazepam use produces physical dependence. Withdrawal syndrome is consistent with the benzodiazepine class — anxiety, insomnia, tremor, and risk of tonic-clonic seizures. The intermediate half-life produces withdrawal dynamics somewhere between short-acting compounds (more rapid, more acute) and ultra-long-acting compounds (slower onset, more prolonged).
Legal Risk
In the United States, possession of flunitrazepam (even without evidence of intent to use for assault) carries significant federal criminal penalties. The illegality of importation and possession creates additional legal risk for individuals obtaining it through illicit channels.
Interaction Profile
- Alcohol — Synergistic CNS depression; increases amnesia and respiratory depression risk substantially
- Opioids — High-risk combination
- Other CNS depressants — Additive effects
Addiction Potential
extremely physically and psychologically addictive
Overdose Information
overdose is a medical emergency that may lead to a coma, permanent brain injury or death if not treated promptly and appropriately.
Symptoms of a benzodiazepine overdose may include severe thought deceleration, slurred speech, confusion, delusions, respiratory depression, coma or death. Benzodiazepine overdoses may be treated effectively in a hospital environment, with generally favorable outcomes. Benzodiazepine overdoses are sometimes treated with flumazenil, a GABAA antagonist. However, care is primarily supportive in nature.
International: Flunitrazepam is a Schedule III drug under the international Convention on Psychotropic Substances of 1971.
Australia: Flunitrazepam is a Schedule 8 (S8) or controlled drug.
Austria:** Flunitrazepam is legal for medical use under the AMG (Arzneimittelgesetz Österreich) and illegal when sold or possessed without a prescription under the SMG (Suchtmittelgesetz Österreich).
Canada: Flunitrazepam is a Schedule I controlled substance and is available by prescription only.
Germany: Since November 2011, flunitrazepam is controlled under Anlage 3 of the BtMG and requires a special prescription.
Switzerland: Flunitrazepam is listed as a controlled narcotic substance, but it is also sparesly prescribed as a sleep aid in major cases. Flunitrazolam tablets only come in 1mg dosage and are dyed green and blue which colors one's mouth notably when ingested in a dissolved beverage.
United Kingdom: Flunitrazepam is a Class C, Schedule 4 controlled drug under the Misuse of Drugs Regulations 2001.
United States: Flunitrazepam is a Schedule IV drug under the Controlled Substances Act in the U.S but is not medically used.
Responsible use
Volumetric liquid dosing
Psychoactive substance index
Flunitrazolam
Temazepam
Depressants
Flunitrazepam (Wikipedia)
Flunitrazepam (Erowid Vault)
Flunitrazepam (Isomer Design)
Flunitrazepam (DrugBank)
=
Dangerous Interactions
The combinations listed below may be life-threatening. Independent research should always be conducted to ensure safety when combining substances.
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Unpredictable potentiation of CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Unpredictable potentiation of CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Compounding CNS depression with anticholinergic effects; risk of cardiac events and respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Unpredictable potentiation of CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Severe respiratory depression; this combination is the leading cause of prescription drug overdose deaths
Combined CNS depression; risk of respiratory failure
Combined CNS depression; risk of respiratory failure
Tolerance
| Full | within a couple of days of continuous use |
| Half | Unknown |
| Zero | 7 - 14 days |
Cross-tolerances
Legal Status
International: Flunitrazepam is a Schedule III drug under the international Convention on Psychotropic Substances of 1971.
Australia: Flunitrazepam is a Schedule 8 (S8) or controlled drug.
Austria:** Flunitrazepam is legal for medical use under the AMG (Arzneimittelgesetz Österreich) and illegal when sold or possessed without a prescription under the SMG (Suchtmittelgesetz Österreich).
Canada: Flunitrazepam is a Schedule I controlled substance and is available by prescription only.
Germany: Since November 2011, flunitrazepam is controlled under Anlage 3 of the BtMG and requires a special prescription.
Switzerland: Flunitrazepam is listed as a controlled narcotic substance, but it is also sparesly prescribed as a sleep aid in major cases. Flunitrazolam tablets only come in 1mg dosage and are dyed green and blue which colors one's mouth notably when ingested in a dissolved beverage.
United Kingdom: Flunitrazepam is a Class C, Schedule 4 controlled drug under the Misuse of Drugs Regulations 2001.
United States: Flunitrazepam is a Schedule IV drug under the Controlled Substances Act in the U.S but is not medically used.
Responsible use
Volumetric liquid dosing
Psychoactive substance index
Flunitrazolam
Temazepam
Depressants
Flunitrazepam (Wikipedia)
Flunitrazepam (Erowid Vault)
Flunitrazepam (Isomer Design)
Flunitrazepam (DrugBank)
Tips (4)
Rebound anxiety after Flunitrazepam wears off is often worse than the original anxiety. This drives a cycle of increasing use. Consider non-pharmacological anxiety management (therapy, exercise, meditation) as primary tools.
Keep a written log of your Flunitrazepam use including time and dose. Benzodiazepines impair memory formation, making it easy to forget you already dosed and accidentally take more. This is how many accidental overdoses happen.
Research chemical benzodiazepines (clonazolam, flualprazolam, etc.) are significantly more potent than pharmaceutical Flunitrazepam. Doses measured in micrograms can cause multi-day blackouts. Use volumetric dosing.
Benzodiazepine withdrawal from Flunitrazepam can be life-threatening. Seizures, psychosis, and death are possible when quitting abruptly after regular use. Always taper gradually under medical supervision. Never cold turkey.
See Also
References (3)
- PubChem: Flunitrazepam
PubChem compound page for Flunitrazepam (CID: 3380)
pubchem - Flunitrazepam - TripSit Factsheet
TripSit factsheet for Flunitrazepam
tripsit - Flunitrazepam - Wikipedia
Wikipedia article on Flunitrazepam
wikipedia