Ziprasidone

Ziprasidone, sold under the brand name Geodon among others, is an atypical antipsychotic used to treat schizophrenia and bipolar disorder.[3] It may be used by mouth and by injection into a muscle (IM).[3] The IM form may be used for acute agitation in people with schizophrenia.[3]

Ziprasidone
Clinical data
Trade namesGeodon, Zeldox, Zipwell, other
AHFS/Drugs.comMonograph
MedlinePlusa699062
License data
Pregnancy
category
  • AU: B3
  • US: C (Risk not ruled out)
    Routes of
    administration    		Oral (capsules), intramuscular injection (IM)
    ATC code
    Legal status
    Legal status
    Pharmacokinetic data
    Bioavailability60% (oral)[1]
    100% (IM)
    MetabolismLiver (aldehyde reductase)
    Elimination half-life7 to 10 hours[2]
    ExcretionUrine and feces
    Identifiers
    CAS Number
    PubChem CID
    IUPHAR/BPS
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEBI
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.106.954
    Chemical and physical data
    FormulaC21H21ClN4OS
    Molar mass412.94 g·mol−1
    3D model (JSmol)
      (verify)

    Common side effects include dizziness, drowsiness, dry mouth, and twitches.[4][5] Although it can also cause weight gain, the risk is much lower than for other antipsychotics.[6] How it works is not entirely clear but is believed to involve effects on serotonin and dopamine in the brain.[3]

    Ziprasidone was approved for medical use in the United States in 2001.[3] The pills are made up of the hydrochloride salt, ziprasidone hydrochloride. The intramuscular form is the mesylate, ziprasidone mesylate trihydrate, and is provided as a lyophilized powder. In 2017, it was the 261st most commonly prescribed medication in the United States, with more than one million prescriptions.[7][8]

    Medical uses

    Ziprasidone is approved by the U.S. Food and Drug Administration (FDA) for the treatment of schizophrenia as well as acute mania and mixed states associated with bipolar disorder. Its intramuscular injection form is approved for acute agitation in schizophrenic patients for whom treatment with just ziprasidone is appropriate.[9]

    In a 2013 study in a comparison of 15 antipsychotic drugs in effectiveness in treating schizophrenic symptoms, ziprasidone demonstrated mild-standard effectiveness. 15% more effective than lurasidone and iloperidone, approximately as effective as chlorpromazine and asenapine, and 9-13% less effective than haloperidol, quetiapine, and aripiprazole.[10] Ziprasidone is effective in the treatment of schizophrenia, though evidence from the CATIE trials suggests it is less effective than olanzapine, and equally as effective compared to quetiapine. There are higher discontinuation rates for lower doses of ziprasidone, which are also less effective than higher doses.[11]

    Adverse effects

    Ziprasidone (and all other second generation antipsychotics (SGAs)) received a black box warning due to increased mortality in elderly patients with dementia-related psychosis.[12]

    Sleepiness and headache are very common adverse effects (>10%).[4][5]

    Common adverse effects (1–10%), include producing too much saliva or having dry mouth, runny nose, respiratory disorders or coughing, nausea and vomiting, stomach aches, constipation or diarrhea, loss of appetite, weight gain (but the smallest risk for weight gain compared to other antipsychotics[6]), rashes, fast heart beats, blood pressure falling when standing up quickly, muscle pain, weakness, twitches, dizziness, and anxiety.[4][5] Extrapyramidal symptoms are also common and include tremor, dystonia (sustained or repetitive muscle contractions), akathisia (the feeling of a need to be in motion), parkinsonism, and muscle rigidity; in a 2013 meta-analysis of 15 antipsychotic drugs, ziprasidone ranked 8th for such side effects.[13]

    Ziprasidone is known to cause activation into mania in some bipolar patients.[14][15][16]

    This medication can cause birth defects, according to animal studies, although this side effect has not been confirmed in humans.[12]

    Recently, the FDA required the manufacturers of some atypical antipsychotics to include a warning about the risk of hyperglycemia and Type II diabetes with atypical antipsychotics. Some evidence suggests that ziprasidone does not cause insulin resistance to the degree of other atypical antipsychotics, such as olanzapine. Weight gain is also less of a concern with ziprasidone compared to other atypical antipsychotics.[17][18][19][20] In fact, in a trial of long term therapy with ziprasidone, overweight patients (BMI > 27) actually had a mean weight loss overall.[12] According to the manufacturer insert, ziprasidone caused an average weight gain of 2.2 kg (4.8 lbs), which is significantly lower than other atypical antipsychotics, making this medication better for patients that are concerned about their weight. In December 2014, the FDA warned that ziprasidone could cause a potentially fatal skin reaction, Drug Reaction with Eosinophilia and Systemic Symptoms, although this was believed to occur only rarely.[21]

    Discontinuation

    The British National Formulary recommends a gradual withdrawal when discontinuing antipsychotics to avoid acute withdrawal syndrome or rapid relapse.[22] Symptoms of withdrawal commonly include nausea, vomiting, and loss of appetite.[23] Other symptoms may include restlessness, increased sweating, and trouble sleeping.[23] Less commonly there may be a feeling of the world spinning, numbness, or muscle pains.[23] Symptoms generally resolve after a short period of time.[23]

    There is tentative evidence that discontinuation of antipsychotics can result in psychosis.[24] It may also result in reoccurrence of the condition that is being treated.[25] Rarely tardive dyskinesia can occur when the medication is stopped.[23]

    Pharmacology

    Pharmacodynamics
    See also: Atypical antipsychotic § Pharmacodynamics, and Antipsychotic § Comparison of medications
    Ziprasidone[26]
    SiteKi (nM)ActionRef
    SERT112Blocker[26]
    NET44Blocker[26]
    DAT>10,000ND[26]
    5-HT1A2.5–76Partial agonist[27][28][29]
    5-HT1B0.99–4.0Partial agonist[28][26]
    5-HT1D5.1–9.0Partial agonist[28][26]
    5-HT1E360–1,279ND[28][26]
    5-HT2A0.08–1.4Antagonist[30][27][28]
    5-HT2B27.2Antagonist[26]
    5-HT2C0.72–13Partial agonist[27]
    5-HT3>10,000ND[26]
    5-HT5A291ND[26]
    5-HT661–76Antagonist[29][27]
    5-HT76.0–9.3Antagonist[26][29][27]
    α1A18Antagonist[26][29]
    α1B9.0Antagonist[26]
    α2A160Antagonist[26][28][29]
    α2B48Antagonist[26][28][29]
    α2C59–77Antagonist[26][28][29]
    β1≥2,570ND[28][26]
    β2>10,000ND[28][26]
    D130–130ND[26][27]
    D24.8Antagonist[31][27][29]
    D2L4.6Antagonist[28][32]
    D2S4.2Antagonist[28]
    D37.2Antagonist[31][27][28]
    D40.8–105Antagonist[31][27][26]
    D4.228–39Antagonist[32]
    D4.414.9Antagonist[33]
    D5152ND[26]
    H115–130Antagonist[28][27][26]
    H23,500ND[26]
    H3>10,000ND[26]
    H4>10,000ND[26]
    M1≥300ND[34][26][27]
    M2≥3,000ND[34][26]
    M3≥1,300ND[34][29][26]
    M4≥1,600ND[34][26]
    M5≥1,600ND[34][26]
    σ1110ND[28]
    σ2NDNDND
    Opioid>1,000ND[28]
    nACh>10,000ND[26]
    NMDA
    (PCP)    		>10,000ND[26]
    VDCC>10,000ND[26][28]
    VGSC2,620ND[28]
    hERG169Blocker[35]
    Values are Ki (nM). The smaller the value, the more strongly the drug binds to the site. All data are for human cloned proteins, except H3 (guinea pig), σ1 (guinea pig), opioid (rodent), NMDA/PCP (rat), VDCC, and VGSC.[26]

    Correspondence to clinical effects

    Ziprasidone mostly affects the receptors of dopamine (D2), serotonin (5-HT2A, partially 5-HT1A, 5-HT2C, and 5-HT1D)[1][36][37] and epinephrine/norepinephrine (α1) to a high degree, while of histamine (H1) - moderately.[38][39] It also somewhat inhibits reuptake of serotonin and norepinephrine, though not dopamine.[38][40]

    Ziprasidone's efficacy in treating the positive symptoms of schizophrenia is believed to be mediated primarily via antagonism of the dopamine receptors, specifically D2. Blockade of the 5-HT2A receptor may also play a role in its effectiveness against positive symptoms, though the significance of this property in antipsychotic drugs is still debated among researchers.[41] Blockade of 5-HT2A and 5-HT2C and activation of 5-HT1A as well as inhibition of the reuptake of serotonin and norepinephrine may all contribute to its ability to alleviate negative symptoms.[42] The relatively weak antagonistic actions of ziprasidone on the α1-adrenergic receptor likely in part explains some of its side effects, such as orthostatic hypotension. Unlike many other antipsychotics, ziprasidone has no significant affinity for the mACh receptors, and as such lacks any anticholinergic side effects. Like most other antipsychotics, ziprasidone is sedating due primarily to serotonin and dopamine blockade.[43][44]

    Pharmacokinetics

    The systemic bioavailability of ziprasidone is 100% when administered intramuscularly and 60% when administered orally without food.[1]

    After a single dose intramuscular administration, the peak serum concentration typically occurs at about 60 minutes after the dose is administered, or earlier.[45] Steady state plasma concentrations are achieved within one to three days. Exposure increases in a dose-related manner and following three days of intramuscular dosing, little accumulation is observed.

    Ziprasidone absorption is optimally achieved when administered with food. Without a meal preceding dose, the bioavailability of the drug is reduced by approximately 50%.[12][46]

    Ziprasidone is hepatically metabolized by aldehyde oxidase; minor metabolism occurs via cytochrome P450 3A4 (CYP3A4).[47] Medications that induce (e.g. carbamazepine) or inhibit (e.g. ketoconazole) CYP3A4 have been shown to decrease and increase, respectively, blood levels of ziprasidone.[48][49]

    Its biological half-life time is 10 hours at doses of 80-120 milligrams.[2]

    History

    Ziprasidone is chemically similar to risperidone,[50] of which it is a structural analogue.[51] It was first synthesized in 1987[52] at the Pfizer central research campus in Groton, Connecticut.[53]

    Phase I trials started in 1995.[54] In 1998 ziprasidone was approved in Sweden.[55][56] After the FDA raised concerns about long QT syndrome, more clinical trials were conducted and submitted to the FDA, which approved the drug on February 5, 2001.[54][57][58]

    Society and culture

    Lawsuit

    In September 2009, the U.S. Justice Department announced that Pfizer had been ordered to pay a historic fine of $2.3 billion as a penalty for fraudulent marketing of several drugs, including Geodon.[59] Pfizer had illegally promoted Geodon and caused false claims to be submitted to government health care programs for uses that were not medically accepted indications. The civil settlement also resolves allegations that Pfizer paid kickbacks to health care providers to induce them to prescribe Geodon, as well as other drugs. This was the largest civil fraud settlement in history against a pharmaceutical company.

    gollark: You know what else isn't useful? `Ultramonad`.
    gollark: Just like Go!
    gollark: ```haskellclass Monad u => Ultramonad u where something :: u a thisIsStupid :: IO a -> u b```
    gollark: NOOOO! EVERYTHING IS A MONAD!
    gollark: ```haskellclass Ultramonad um where ultrabind :: um (um a) -> (a -> um (um b)) ultrareturn :: a -> um (um a)```

    References
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    Further reading
    • David Taylor (2006). Schizophrenia in Focus. Pharmaceutical Press. p. 123. ISBN 978-0-85369-607-0. Retrieved May 13, 2012.
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