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| Clinical data | |
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| Trade names | Prolixin, Modecate, Moditen others |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a682172 |
| License data | |
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| Routes of administration | By mouth,Intramuscular injection, depot injection (fluphenazine decanoate) |
| Drug class | Typical antipsychotic |
| ATC code | |
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| Pharmacokinetic data | |
| Bioavailability | 2.7% (by mouth) |
| Metabolism | unclear[2] |
| Eliminationhalf-life | IM 15 hours (HCl), 7–10 days (decanoate)[2] |
| Excretion | Urine, feces |
| Identifiers | |
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| CAS Number |
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| IUPHAR/BPS | |
| DrugBank |
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| CompTox Dashboard(EPA) | |
| ECHA InfoCard | 100.000.639 |
| Chemical and physical data | |
| Formula | C22H26F3N3OS |
| Molar mass | 437.53 g·mol−1 |
| 3D model (JSmol) | |
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Fluphenazine, sold under the brand nameProlixin among others, is a high-potency typicalantipsychotic medication.[2] It is used in the treatment of chronicpsychoses such asschizophrenia,[2][3] and appears to be about equal in effectiveness to low-potencyantipsychotics likechlorpromazine.[4] It is givenby mouth,injection into a muscle, orjust under the skin.[2] There is also a long acting injectable version that may last for up to four weeks.[2] Fluphenazine decanoate, thedepot injection form of fluphenazine, should not be used by people with severe depression.[5][6]
Common side effects includemovement problems,sleepiness,depression andincreased weight.[2] Serious side effects may includeneuroleptic malignant syndrome,low white blood cell levels, and the potentially permanent movement disordertardive dyskinesia.[2] In older people with psychosis as a result ofdementia it may increase the risk of dying.[2] It may also increaseprolactin levels which may result inmilk production,enlarged breasts in males,impotence, andthe absence of menstrual periods.[2] It is unclear if it is safe for use inpregnancy.[2]
Fluphenazine is atypical antipsychotic of thephenothiazine class.[2] Its mechanism of action is not entirely clear but believed to be related to its ability toblock dopamine receptors.[2] In up to 40% of those on long term phenothiazines, liver function tests become mildly abnormal.[7]
Fluphenazine inhibitstubulin polymerization, a property shared with otherphenothiazine derivatives includingperphenazine,chlorpromazine,trifluoperazine, andtriflupromazine.[8]
Fluphenazine came into use in 1959.[9] The injectable form is on theWorld Health Organization's List of Essential Medicines.[10] It is available as ageneric medication.[2] It was discontinued in Australia in 2017.[11]
A 2018Cochrane review found that fluphenazine was an imperfect treatment and other inexpensive drugs less associated with side effects may be an equally effective choice for people withschizophrenia.[12] Another 2018 Cochrane review found that there was limited evidence that neweratypical antipsychotics were more tolerable than fluphenazine.[13] Intramusculardepot injection forms are available as both thedecanoate andenanthate esters.[14]
TheBritish National Formulary recommends a gradual withdrawal when discontinuing antipsychotics to avoid acute withdrawal syndrome or rapid relapse.[15] Symptoms of withdrawal commonly include nausea, vomiting, and loss of appetite.[16] Other symptoms may include restlessness, increased sweating, and trouble sleeping.[16] Less commonly there may be a feeling of the world spinning, numbness, or muscle pains.[16] Symptoms generally resolve after a short period of time.[16]
There is tentative evidence that discontinuation of antipsychotics can result in psychosis.[17] It may also result in reoccurrence of the condition that is being treated.[18] Rarely tardive dyskinesia can occur when the medication is stopped.[16]
Fluphenazine acts primarily by blocking post-synaptic dopaminergic D2 receptors in the basal ganglia, cortical and limbic system. It also blocks α1 adrenergic receptors, muscarinic M1 receptors, and histaminergic H1 receptors.[19][20]
| Target | Ki (nM) | Action |
|---|---|---|
| 5-HT1A | 145–2829 | ND |
| 5-HT1B | 334 | Modulator |
| 5-HT1D | 334 | ND |
| 5-HT1E | 540 | ND |
| 5-HT2A | 3.8–98 | Antagonist |
| 5-HT2C | 174–2,570 | Antagonist |
| 5-HT3 | 4,265– >10,000 | ND |
| 5-HT5A | 145 | ND |
| 5-HT6 | 7.9–38 | ND |
| 5-HT7 | 8 | ND |
| D1 | 14.45 | Antagonist |
| D2 | 0.89 | Antagonist |
| D2L | 0.50 | ND |
| D3 | 1.412 | ND |
| D4 | 89.12 | ND |
| D5 | 95–2,590 | ND |
| α1A | 6.4–9 | Antagonist |
| α1B | 13 | ND |
| α2A | 304–314 | ND |
| α2B | 181.6–320 | ND |
| α2C | 28.8–122 | ND |
| β1 | >10,000 | ND |
| β2 | >10,000 | ND |
| H1 | 7.3–70 | Antagonist |
| H2 | 560 | ND |
| H3 | 1,000 | ND |
| H4 | >10,000 | ND |
| M1 | 1,095-3,235.93 | Antagonist |
| M2 | 2,187.76–7,163 | ND |
| M3 | 1441–1445.4 | ND |
| M4 | 5,321 | ND |
| M5 | 357 | ND |
| SERTTooltip Serotonin transporter | 5,950 | ND |
| NETTooltip Norepinephrine transporter | 3,076–4,100 | ND |
| DATTooltip Dopamine transporter | 10,000–11,000 | ND |
| NMDA (PCP) | >10,000 | ND |
| The smaller the Ki, the more strongly the drug binds to the site. All data are for human cloned proteins, except 5-HT3 (rat), D4 (human/rat), H3 (guinea pig), and NMDA/PCP (rat).[21] | ||
Oral fluphenazine rapidlyabsorbs withplasma levels peaking at 2 hours post-ingestion.[24] Thehalf-life is about 15-16 hours.[24][25]Steady state concentrations vary considerably across individuals, which indicates variability in absorption,metabolism, orexcretion.[24] Additionally, the dose-level relationship is curvilinear with plasma levels of 0.2 - 2.8 ng/mL being optimal for clinical improvement.[24]Benztropine mesylate did not indicate any major drug-drug interactions.[24]
| Medication | Brand name | Class | Vehicle | Dosage | Tmax | t1/2 single | t1/2 multiple | logPc | Ref |
|---|---|---|---|---|---|---|---|---|---|
| Aripiprazole lauroxil | Aristada | Atypical | Watera | 441–1064 mg/4–8 weeks | 24–35 days | ? | 54–57 days | 7.9–10.0 | |
| Aripiprazole monohydrate | Abilify Maintena | Atypical | Watera | 300–400 mg/4 weeks | 7 days | ? | 30–47 days | 4.9–5.2 | |
| Bromperidol decanoate | Impromen Decanoas | Typical | Sesame oil | 40–300 mg/4 weeks | 3–9 days | ? | 21–25 days | 7.9 | [26] |
| Clopentixol decanoate | Sordinol Depot | Typical | Viscoleob | 50–600 mg/1–4 weeks | 4–7 days | ? | 19 days | 9.0 | [27] |
| Flupentixol decanoate | Depixol | Typical | Viscoleob | 10–200 mg/2–4 weeks | 4–10 days | 8 days | 17 days | 7.2–9.2 | [27][28] |
| Fluphenazine decanoate | Prolixin Decanoate | Typical | Sesame oil | 12.5–100 mg/2–5 weeks | 1–2 days | 1–10 days | 14–100 days | 7.2–9.0 | [29][30][31] |
| Fluphenazine enanthate | Prolixin Enanthate | Typical | Sesame oil | 12.5–100 mg/1–4 weeks | 2–3 days | 4 days | ? | 6.4–7.4 | [30] |
| Fluspirilene | Imap, Redeptin | Typical | Watera | 2–12 mg/1 week | 1–8 days | 7 days | ? | 5.2–5.8 | [32] |
| Haloperidol decanoate | Haldol Decanoate | Typical | Sesame oil | 20–400 mg/2–4 weeks | 3–9 days | 18–21 days | 7.2–7.9 | [33][34] | |
| Olanzapine pamoate | Zyprexa Relprevv | Atypical | Watera | 150–405 mg/2–4 weeks | 7 days | ? | 30 days | – | |
| Oxyprothepin decanoate | Meclopin | Typical | ? | ? | ? | ? | ? | 8.5–8.7 | |
| Paliperidone palmitate | Invega Sustenna | Atypical | Watera | 39–819 mg/4–12 weeks | 13–33 days | 25–139 days | ? | 8.1–10.1 | |
| Perphenazine decanoate | Trilafon Dekanoat | Typical | Sesame oil | 50–200 mg/2–4 weeks | ? | ? | 27 days | 8.9 | |
| Perphenazine enanthate | Trilafon Enanthate | Typical | Sesame oil | 25–200 mg/2 weeks | 2–3 days | ? | 4–7 days | 6.4–7.2 | [35] |
| Pipotiazine palmitate | Piportil Longum | Typical | Viscoleob | 25–400 mg/4 weeks | 9–10 days | ? | 14–21 days | 8.5–11.6 | [28] |
| Pipotiazine undecylenate | Piportil Medium | Typical | Sesame oil | 100–200 mg/2 weeks | ? | ? | ? | 8.4 | |
| Risperidone | Risperdal Consta | Atypical | Microspheres | 12.5–75 mg/2 weeks | 21 days | ? | 3–6 days | – | |
| Zuclopentixol acetate | Clopixol Acuphase | Typical | Viscoleob | 50–200 mg/1–3 days | 1–2 days | 1–2 days | 4.7–4.9 | ||
| Zuclopentixol decanoate | Clopixol Depot | Typical | Viscoleob | 50–800 mg/2–4 weeks | 4–9 days | ? | 11–21 days | 7.5–9.0 | |
| Note: All byintramuscular injection.Footnotes:a =Microcrystalline ornanocrystallineaqueous suspension.b = Low-viscosityvegetable oil (specificallyfractionated coconut oil withmedium-chain triglycerides).c = Predicted, fromPubChem andDrugBank.Sources:Main: See template. | |||||||||
Fluphenazine came into use in 1959.[9]
The injectable form is on theWorld Health Organization's List of Essential Medicines.[10] It is available as ageneric medication.[2] It was discontinued in Australia in 2017.[11]
In horses, it is sometimes given by injection as ananxiety-relieving medication, though there are many negative common side effects and it is forbidden by many equestrian competition organizations.[36]
Withdrawal of antipsychotic drugs after long-term therapy should always be gradual and closely monitored to avoid the risk of acute withdrawal syndromes or rapid relapse.
