Prescription medication · Atypical Antipsychotic
ziprasidone
Also sold as Geodon. Ziprasidone treats schizophrenia in adults.
Data updated 2026-05-15
- 17,328
- FDA reportsModerately reported
- 18
- InteractionsSeveral interactions
- 99% less
- Generic vs brandHuge savings
- $23.92
- Brand price (NADAC)
What the data shows
ziprasidone (Geodon) is a prescription Atypical Antipsychotic, reported at a middle-of-the-pack volume (17,328 FDA reports), whose generic costs a fraction of the brand (about 99% less).
Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.
ziprasidone (Geodon) is a prescription Atypical Antipsychotic. Ziprasidone treats schizophrenia in adults.
Ziprasidone is a medicine used to treat mental disorders. It helps to balance chemicals in the brain to improve mood and behavior.
Verify with FDA → · CMS NADAC pricing →
Drug Pricing (NADAC)
Brand Price
$23.92/unit
Generic Price
$0.23/unit
Generic Savings
99%
Generic Available
Yes (8 manufacturers)
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
Ziprasidone treats schizophrenia in adults.
Common side effects
Feeling sleepy, Respiratory tract infection, Extrapyramidal symptoms (movement problems)
Key warnings
This medicine may increase the risk of death in elderly patients who have psychosis related to dementia.
The sections below are summarized in plain English from ziprasidone's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Ziprasidone is an atypical antipsychotic. It works by affecting certain chemicals in the brain, like dopamine and serotonin. By balancing these chemicals, it helps to reduce symptoms of mental illness.
How to Take It
Take ziprasidone capsules by mouth with food. Swallow the capsules whole; do not crush, open, or chew them. For schizophrenia, you may start with 20 mg twice a day. Your doctor may adjust the dose up to 80 mg twice a day, but no sooner than every 2 days.
This is a plain-language summary of ziprasidone's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
Tell your doctor if you are pregnant or plan to become pregnant. Babies born to mothers who use this medicine in the last 3 months of pregnancy may have withdrawal symptoms after birth. There is a pregnancy registry, call 1-866-961-2388.
This is a plain-language summary of ziprasidone's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
Missed Dose
If you miss a dose, take it as soon as you remember. If it is close to your next dose, skip the missed dose and continue with your regular schedule.
This is a plain-language summary of ziprasidone's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store ziprasidone capsules at room temperature, between 68° to 77°F (20° to 25°C).
Side Effects (from patient reports)
Based on 17,328 FDA adverse event reports.
Most-reported reactions
Adverse reactions in FAERS for ziprasidone, by number of reports
- Gaining weight
Gaining weight
1,176 reports
- Diabetes
Diabetes
1,003 reports
- Feeling anxious
Feeling anxious
875 reports
- Type 2 diabetes
Type 2 diabetes
859 reports
- Trouble sleeping
Trouble sleeping
801 reports
- Feeling depressed
Feeling depressed
782 reports
- Feeling sleepy
Feeling sleepy
745 reports
- Feeling tired
Feeling tired
719 reports
- Movement disorder
Movement disorder
700 reports
- Shaking
Shaking
686 reports
What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.
Reports over time
Adverse-event reports filed for ziprasidone each year to the FDA Adverse Event Reporting System (FAERS).
Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.
Where ziprasidone sits
ziprasidone has more FDA adverse-event reports than 52% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.
Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is ziprasidone; the line is the median (50th percentile).
FDA Adverse Event Report Analysis
Detailed analysis of 17,328 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.
Total Reports
17,328
Reports Mentioning Death
1,171
6.8% of reports — not proof of cause
Hospitalization Reports
4,189
Top Indication
Bipolar Disorder
Gender Distribution
Age Distribution
Most Reported Adverse Reactions (FAERS)
| # | Reaction | Reports |
|---|---|---|
| 2 | WEIGHT INCREASED | 1,176 |
| 3 | DIABETES MELLITUS | 1,003 |
| 4 | ANXIETY | 875 |
| 5 | TYPE 2 DIABETES MELLITUS | 859 |
| 6 | INSOMNIA | 801 |
| 7 | DEPRESSION | 782 |
| 8 | SOMNOLENCE | 744 |
| 9 | FATIGUE | 719 |
| 10 | TARDIVE DYSKINESIA | 700 |
| 11 | TREMOR | 686 |
| 12 | NAUSEA | 673 |
| 13 | DIZZINESS | 587 |
| 14 | FEELING ABNORMAL | 587 |
| 15 | SUICIDAL IDEATION | 568 |
| 16 | HEADACHE | 554 |
Reactions in Death Reports
Reactions in Hospitalization Reports
Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation
Serious Warnings
This medicine may increase the risk of death in elderly patients who have psychosis related to dementia. Ziprasidone is not approved to treat dementia-related psychosis. Talk to your doctor about the risks if you are an elderly patient with dementia.
Known Drug Interactions
Risk of serotonin syndrome with concomitant therapy with other serotonergic drugs such as SNRIs, SSRIs, triptans, tricyclic antidepressants, opioids, lithium, tryptophan, buspirone, amphetamines, and St.
Mechanism: Both of these drugs increase a chemical in the brain called serotonin. Having too much serotonin can lead to a dangerous condition called serotonin syndrome.
What to do: Tell your doctor if you feel very restless, confused, or have a fast heartbeat. Your doctor will decide if it is safe for you to take both medicines.
Risk of serotonin syndrome with concomitant therapy with other serotonergic drugs such as SNRIs, SSRIs, triptans, tricyclic antidepressants, opioids, lithium, tryptophan, buspirone, amphetamines, and St. 7.5 Lithium Ziprasidone at a dose of 40 mg twice daily administered concomitantly with lithium at a dose of 450 mg twice daily for 7 days did not affect the steady-state level or renal clearance of lithium. Ziprasidone dosed adjunctively to lithium in a maintenance trial of bipolar patients did not affect mean therapeutic lithium levels.
Mechanism: These drugs can both raise serotonin levels in the body. When used together, they may cause a serious reaction called serotonin syndrome.
What to do: Your doctor should monitor you for symptoms like muscle stiffness or fever. Do not stop taking your medicine without talking to your provider first.
7.5 Drugs That Cause QTc Prolongation Tetrabenazine causes a small prolongation of QTc (about 8 msec), concomitant use with other drugs that are known to cause QTc prolongation should be avoided, these including antipsychotic medications (e.g., chlorpromazine, haloperidol, thioridazine, ziprasidone), antibiotics (e.g., moxifloxacin), Class 1A (e.g., quinidine, procainamide) and Class III (e.g., amiodarone, sotalol) antiarrhythmic medications or any other medications known to prolong the QTc interval. 7.6 Neuroleptic Drugs The risk for Parkinsonism, NMS, and akathisia may be increased by...
Mechanism: Both drugs can cause a dangerous change in the heart's rhythm and increase the risk of serious movement problems.
What to do: You should avoid taking these drugs together to prevent heart rhythm issues and severe muscle side effects.
Ziprasidone at a dose of 20 mg twice daily did not affect the pharmacokinetics of concomitantly administered oral contraceptives, ethinyl estradiol (0.03 mg) and levonorgestrel (0.15 mg).
Mechanism: Ziprasidone does not change the way the body breaks down or removes estradiol from the system. This means the levels of the hormone in your blood stay the same.
What to do: You can safely take these medications together without needing to adjust your dose. Your birth control or hormone therapy should work as expected.
7.9 Other Concomitant Drug Therapy Population pharmacokinetic analysis of schizophrenic patients enrolled in controlled clinical trials has not revealed evidence of any clinically significant pharmacokinetic interactions with benztropine, propranolol, or lorazepam.
Mechanism: Studies of patients show that these two drugs do not have a significant effect on how the body handles either medication. They do not change each other's levels in the body.
What to do: No special precautions or dose changes are typically required when using these drugs at the same time.
This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.
Common Questions
Can I take ziprasidone without food?
What should I do if I feel worse after starting ziprasidone?
Can I drive while taking ziprasidone?
How long does it take for ziprasidone to start working?
Can I stop taking ziprasidone suddenly?
Does ziprasidone interact with other medications?
What if I experience side effects?
Can ziprasidone cause weight gain?
Is ziprasidone addictive?
What should I avoid while taking ziprasidone?
What are the common side effects of ziprasidone?
Does ziprasidone interact with other medications?
What drug class is ziprasidone?
Is there a generic version of ziprasidone?
Is ziprasidone safe during pregnancy?
Related Medications in Atypical Antipsychotic
Other drugs grouped near ziprasidone - same-class peers and common alternatives.
acamprosate
Campral
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alprazolam
Xanax
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amitriptyline
Elavil
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amphetamine/dextroamphetamine
Adderall, Adderall XR
Adderall XR is a stimulant medicine.
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aripiprazole
Abilify
Aripiprazole (Abilify) is a medicine used to treat certain mental disorders and mood problems.
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Medication Guides
Understanding Drug Interactions
How CYP450 enzymes, inhibitors, and inducers affect your medications
Generic vs Brand Name Drugs
FDA requirements, cost savings, and when the difference matters
Narrow Therapeutic Index Drugs
Why some drugs demand precise dosing and monitoring
Common Drug Interactions
Dangerous medication combinations and how to protect yourself
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What the FDA Data Shows for ziprasidone
The FDA label for ziprasidone (sold under brand names such as Geodon) classifies it as a prescription-only medication in the Atypical Antipsychotic class. Ziprasidone treats schizophrenia in adults. Official labeling lists 8 commonly reported side effects, including Feeling sleepy, Respiratory tract infection, Extrapyramidal symptoms (movement problems).
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 17,328 voluntary reports. The database also lists 18 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS shows a generic unit cost of $0.23 versus $23.92 for the brand - a 99% generic savings.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: April 5, 2025
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages