Prescription medication · Vasopressin Receptor Agonist

vasopressin

Also sold as Vasostrict. Vasopressin injection is used to increase blood pressure.

Data updated 2026-05-15

4,135
FDA reportsLightly reported
9
InteractionsFew interactions
2
Recall records

What the data shows

vasopressin (Vasostrict) is a prescription Vasopressin Receptor Agonist, among the least-reported drugs the FDA tracks (4,135 FDA reports), with 9 documented drug interactions.

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.

vasopressin (Vasostrict) is a prescription Vasopressin Receptor Agonist. Vasopressin injection is used to increase blood pressure.

Vasopressin injection helps raise blood pressure in adults with shock. It is used when fluids and other medicines don't work well enough.

Compare with Another Drug → Full Side Effects Report →

What it does

Vasopressin injection is used to increase blood pressure.

Common side effects

Decreased heart output, Slow heart rate, Fast or irregular heart rate

Key warnings

Vasopressin can worsen heart function.

The sections below are summarized in plain English from vasopressin's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Vasopressin is a hormone that makes blood vessels get tighter. This helps to increase blood pressure. It can also affect how your kidneys handle water.

Side Effects (from patient reports)

Based on 4,135 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for vasopressin, by number of reports

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.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for vasopressin each year to the FDA Adverse Event Reporting System (FAERS).

0200400600800 20042007201020132016201920222025 508

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where vasopressin sits

vasopressin has more FDA adverse-event reports than 23% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is vasopressin; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 4,135 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

4,135

Reports Mentioning Death

1,633

39.5% of reports — not proof of cause

Hospitalization Reports

2,378

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 1,600 (42%)
Male 2,168 (57%)

Age Distribution

0–17 380
18–44 872
45–64 1,251
65–74 523
75+ 551

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
3 HYPOTENSION 486
4 CARDIOGENIC SHOCK 389
5 SEPSIS 380
6 MULTIPLE ORGAN DYSFUNCTION SYNDROME 375
7 CONDITION AGGRAVATED 359
8 TOXICITY TO VARIOUS AGENTS 317
9 ACUTE KIDNEY INJURY 308
10 STRESS 290
11 VOMITING 289
12 ABDOMINAL PAIN 263
13 HYPONATRAEMIA 260
14 GENERAL PHYSICAL HEALTH DETERIORATION 259
15 NAUSEA 256
16 ASCITES 255
17 ABDOMINAL DISTENSION 250

Reactions in Death Reports

MULTIPLE ORGAN DYSFUNCTION SYNDROME 354
SEPSIS 338
CARDIOGENIC SHOCK 273
STRESS 262
VOMITING 256
GENERAL PHYSICAL HEALTH DETERIORATION 248
ASCITES 247
ABDOMINAL DISTENSION 243
ABDOMINAL PAIN 241
NAUSEA 239

Reactions in Hospitalization Reports

HYPOTENSION 344
TOXICITY TO VARIOUS AGENTS 268
CONDITION AGGRAVATED 253
CARDIOGENIC SHOCK 237
ACUTE KIDNEY INJURY 216
INTENTIONAL OVERDOSE 203
SEPSIS 201
MULTIPLE ORGAN DYSFUNCTION SYNDROME 199
CARDIAC ARREST 164
VOMITING 164

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

Vasopressin can worsen heart function. It can also cause a type of diabetes where you pee a lot. Your doctor will check your electrolytes and urine after you stop taking it.

Known Drug Interactions

Vasopressin receptor antagonists tolvaptan ↑ tolvaptan Co-administration contraindicated due to potential for dehydration, hypovolemia and hyperkalemia [see Contraindications (4) ] .

Mechanism: This combination causes tolvaptan levels to rise because the body cannot get rid of it fast enough. This can lead to severe fluid loss and high potassium levels.

Vasopressin Receptor Antagonists Conivaptan Tolvaptan Not recommended during and 2 weeks after itraconazole treatment.

Mechanism: Itraconazole slows down the process of clearing these medicines from your body. This can lead to higher amounts of the drug in your system and a higher risk of side effects.

minor lithium

7.5 Drugs Suspected of Causing Diabetes Insipidus Use with drugs suspected of causing diabetes insipidus (e.g., demeclocycline, lithium, foscarnet, clozapine) may decrease the pressor effect in addition to the antidiuretic effect of Vasopressin injection.

Mechanism: Lithium can block the effects of vasopressin, making it less able to raise blood pressure or manage water levels.

7.4 Drugs Suspected of Causing SIADH Use with drugs suspected of causing SIADH (e.g., SSRIs, tricyclic antidepressants, haloperidol, chlorpropamide, enalapril, methyldopa, pentamidine, vincristine, cyclophosphamide, ifosfamide, felbamate) may increase the pressor effect in addition to the antidiuretic effect of Vasopressin injection.

Mechanism: Enalapril can cause the body to hold onto more water, which adds to the effects of vasopressin. This can lead to higher blood pressure and more water retention.

7.4 Drugs Suspected of Causing SIADH Use with drugs suspected of causing SIADH (e.g., SSRIs, tricyclic antidepressants, haloperidol, chlorpropamide, enalapril, methyldopa, pentamidine, vincristine, cyclophosphamide, ifosfamide, felbamate) may increase the pressor effect in addition to the antidiuretic effect of Vasopressin injection.

Mechanism: Haloperidol may cause the body to keep too much water, which makes the effects of vasopressin stronger. This can increase blood pressure and water buildup in the body.

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This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

What should I tell my doctor before taking vasopressin?
Tell your doctor if you are allergic to vasopressin. Also, tell them about all your other medical conditions and medicines.
How will I know if the medicine is working?
Your doctor will monitor your blood pressure to see if the medicine is working.
Can vasopressin interact with other medicines?
Yes, vasopressin can interact with other medicines. Tell your doctor about all the medicines you take.
What if I have side effects?
Tell your doctor or nurse right away if you have any side effects.
Will I need any tests while taking vasopressin?
Your doctor will check your blood pressure, electrolytes, and urine output.
Can vasopressin cause diabetes?
Yes, vasopressin can cause a temporary type of diabetes where you pee a lot.
How long will I need to take vasopressin?
Your doctor will decide how long you need to take vasopressin.
What is the strength of this medicine?
Vasopressin injection contains 20 units of vasopressin per 1 mL.
How is vasopressin given?
Vasopressin is given through an IV into your vein.
What should I avoid while taking vasopressin?
Talk to your doctor about any specific things to avoid while taking vasopressin.
What are the common side effects of vasopressin?
The registry lists Decreased heart output, Slow heart rate, Fast or irregular heart rate, Low sodium levels in the blood, Reduced blood flow to the heart among the most-reported FAERS reaction terms for vasopressin. The compiled record contains 4,135 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does vasopressin interact with other medications?
The registry has 9 documented interaction rows for vasopressin. Notable source-record pairings include nirmatrelvir/ritonavir, itraconazole, lithium. These rows are not a complete medication review.
What drug class is vasopressin?
vasopressin belongs to the Vasopressin Receptor Agonist drug class. It requires a prescription (Rx). Vasopressin injection is used to increase blood pressure.
What pregnancy or breastfeeding source fields are listed for vasopressin?
The FDA label for vasopressin contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
Has vasopressin been recalled?
There are 2 recalls associated with vasopressin products. Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date. Check the recalls section below for full details and affected products.

Active Recalls

Class II January 22, 2024

Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.

IntegraDose Compounding Services LLC

Class II January 11, 2024

Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

Par Sterile Products LLC

Other drugs grouped near vasopressin - same-class peers and common alternatives.

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Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for vasopressin: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

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What the FDA Data Shows for vasopressin

The FDA label for vasopressin (sold under brand names such as Vasostrict) classifies it as a prescription-only medication in the Vasopressin Receptor Agonist class. Vasopressin injection is used to increase blood pressure. Official labeling lists 8 commonly reported side effects, including Decreased heart output, Slow heart rate, Fast or irregular heart rate.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 4,135 voluntary reports. The database also lists 9 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.

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 (currently 2 recall records on file), and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.

Last updated: February 15, 2025

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page