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Benadryl Challenge: What FDA Adverse Event Data Shows

We pulled 1,092 FDA FAERS reports for diphenhydramine misuse. The data shows a 2,314% spike in reports during TikTok viral periods, 310 deaths, and a resurgence in 2025-2026.

by MyfitByte(9 min read)

Benadryl Challenge: What FDA Adverse Event Data Shows

FDA adverse event reports for diphenhydramine overdose and misuse Diphenhydramine (Benadryl) adverse event reports spiked 2,314% in 2021 when the TikTok challenge first went viral. Source: FDA FAERS via MyfitByte API.

The Benadryl Challenge keeps coming back. TikTok users dare each other to take large doses of diphenhydramine to hallucinate on camera. The American Academy of Pediatrics presented new data on it in July 2026. News outlets repeat "FDA warns" without showing any actual FDA data.

So we pulled the numbers ourselves. Here's what 1,092 adverse event reports from the FDA's FAERS database reveal about diphenhydramine misuse, overdose, and death.

TL;DR

  • 1,092 total FAERS reports for diphenhydramine linked to adverse events (2018-2025)
  • 310 deaths reported across all age groups, 75 among people 25 and younger
  • 2021 spike: 531 reports (up from 22 in 2020, a 2,314% increase) coinciding with the first TikTok viral wave
  • 2025 was worse: 374 reports for the full year, with 178 deaths recorded
  • 81% of all reports classified as serious (hospitalization, life-threatening, or death)
  • Under-25 age group shows cardiac arrest, seizures, and QT prolongation as top clinical findings

How we got this data

We queried the FDA Adverse Event Reporting System (FAERS) through the MyfitByte API. FAERS collects voluntary reports from healthcare professionals, consumers, and manufacturers about drug side effects submitted to the FDA.

The query:

curl -H "x-api-key: YOUR_KEY" \
  "https://myfitbyte.com/api/v1/adverse-events?drug=diphenhydramine&limit=100"

Important context: FAERS is a passive surveillance system. Reports do not prove causation. Not all adverse events get reported. But trends in report volume, especially sudden spikes tied to known cultural events, are strong signals.

Report volume: two clear viral spikes

Year Reports Deaths Under 18 Age 18-25
2018 3 2 0 0
2019 8 3 0 0
2020 22 7 1 1
2021 531 96 48 43
2022 1 1 0 0
2023 49 13 4 2
2024 104 10 7 5
2025 374 178 27 25

Two patterns stand out.

First: 2021. Reports jumped from 22 to 531 in one year. The Benadryl Challenge first went viral on TikTok in late 2020. By 2021, the reporting system captured the fallout. That 91 under-25 patients appear in a single year for an OTC antihistamine is abnormal by any measure.

Second: 2025. The full year logged 374 reports with 178 deaths, nearly matching 2021's peak volume. The challenge resurfaced hard. The AAP's July 2026 conference presentation confirms what the data already showed months earlier.

What happens to the body: top reported reactions

The clinical picture from FAERS reports paints a consistent overdose toxidrome:

Reaction Reports What it means
Toxicity to various agents 186 Multi-organ poisoning
Completed suicide 121 Intentional fatal overdose
Overdose 100 Excessive dose ingested
Drug abuse 75 Recreational misuse flagged
Hallucination, visual 63 The "desired" effect of the challenge
Intentional overdose 58 Deliberate excessive ingestion
Tachycardia 49 Heart racing dangerously fast
Cardiac arrest 38 Heart stopped
Coma 35 Loss of consciousness
Seizure 29 Brain misfiring from toxicity

The hallucinations that TikTok users chase sit in the same dose range that causes cardiac arrest and seizures. Diphenhydramine is an anticholinergic. At high doses, it blocks acetylcholine receptors throughout the nervous system. The "trip" and the cardiac toxicity are the same pharmacological event at different organ sites.

The under-25 picture is worse

Among patients 25 and younger, the top reported reactions shift toward acute cardiac events:

Reaction Reports (Under 25)
Toxicity to various agents 55
Completed suicide 32
Tachycardia 30
Overdose 28
Cardiac arrest 19
QRS complex prolonged 16
QT prolonged 16
Hypertension 16
Mydriasis (dilated pupils) 15
Seizure 14
Respiratory arrest 13

QRS and QT prolongation are ECG findings that precede fatal arrhythmias. Their appearance in this age group, alongside cardiac arrest and respiratory arrest, shows these are not "bad trips." They are poisoning events.

Outcomes for under-25 patients by year:

Year Deaths Hospitalized Life-Threatening
2020 1 1 0
2021 40 28 4
2023 5 0 0
2024 2 5 0
2025 33 12 0

Forty deaths among under-25s in 2021. Thirty-three in 2025. The trend is not improving.

Who reports these events?

Reporter Count Percentage
Consumer 480 44%
Other health professional 303 28%
Physician 273 25%
Pharmacist 23 2%
Unknown 13 1%

Nearly half come from consumers, which includes family members reporting after a death or hospitalization. The high physician involvement (25%) suggests emergency departments are submitting reports for severe cases.

How diphenhydramine compares to other OTC drugs

Is this spike unique to Benadryl, or did all OTC drug reports increase? We pulled ibuprofen and acetaminophen for context:

Drug 2019 2020 2021 Change (2020-2021)
Diphenhydramine 8 22 463 +2,004%
Ibuprofen 72 102 5,078 +4,878%
Acetaminophen 69 82 1,990 +2,327%

All three OTC drugs show a 2021 spike (likely reflecting a FAERS reporting system change or catch-up from pandemic-era backlogs). But diphenhydramine's ratio of deaths-to-total-reports is far higher. For diphenhydramine: 96 deaths out of 531 reports (18%). For comparison purposes, the death rate in ibuprofen reports over the same period runs under 5%.

Why this keeps happening

Three factors keep the Benadryl Challenge alive:

Accessibility. Diphenhydramine is sold without prescription, without age verification in most states, in packages of 100+ tablets for under $10. A lethal dose costs less than a coffee.

Pharmacology misconception. Users believe "antihistamine" means "safe." The anticholinergic mechanism at high doses produces delirium, not a controlled psychedelic experience. Participants cannot predict or control the outcome.

Platform dynamics. TikTok's algorithm resurfaces challenge content cyclically. Each resurgence creates a new cohort of first-time participants who missed prior warnings. The 2025 data shows this cycle repeating.

What the FDA has done

The FDA issued a safety communication in September 2020 warning about diphenhydramine overdose risks tied to social media challenges. Johnson & Johnson (Benadryl's manufacturer) updated packaging and worked with platforms to remove challenge content.

Neither intervention shows lasting effect in the data. The 2025 numbers nearly matched 2021's totals, and early 2026 reports suggest the cycle continues.

Limitations of this data

FAERS has known constraints that affect interpretation:

  • Underreporting. The FDA estimates FAERS captures only 1-10% of actual adverse events. The true numbers are likely 10-100x higher.
  • No denominator. We know 1,092 reports exist, but not how many people attempted the challenge without incident.
  • Reporting lag. Events from late 2025 and early 2026 may not yet appear in FAERS due to quarterly release cycles.
  • Duplicate reports. The same event can generate reports from both a consumer and their physician.
  • No intent confirmation. A diphenhydramine overdose report does not specify whether it was a TikTok challenge, suicide attempt, or accidental ingestion. We infer challenge involvement from timing and demographics.

FAQ

Is the Benadryl Challenge still happening in 2026?

Yes. FDA FAERS data shows 374 reports in 2025, nearly matching the original 2021 viral wave. The AAP presented new data on the ongoing trend at their July 2026 conference.

How many people have died from the Benadryl Challenge?

FAERS records 310 total deaths linked to diphenhydramine adverse events between 2018 and 2025. Among patients 25 and younger, 75 deaths are recorded. Due to underreporting (FAERS captures an estimated 1-10% of events), actual numbers are likely higher.

What dose of Benadryl is dangerous?

The standard adult dose is 25-50mg. Toxic effects begin around 300-500mg (12-20 tablets). Doses above 1,000mg carry significant risk of cardiac arrest, seizures, and death. The "challenge" dose targets hallucination, which requires toxic-level ingestion.

Why does Benadryl cause hallucinations at high doses?

Diphenhydramine is an anticholinergic. At high doses, it blocks acetylcholine throughout the central nervous system, causing delirium with visual hallucinations. This is not a psychedelic effect. Participants experience confusion, paranoia, and inability to distinguish hallucinations from reality.

Can you buy Benadryl without ID?

In most US states, yes. Diphenhydramine has no purchase restrictions, age verification requirements, or quantity limits at retail. Some retailers have voluntarily placed it behind counters or limited package sizes.

Has the FDA banned large Benadryl packages?

No. The FDA issued a warning in September 2020 but has not restricted package sizes, imposed purchase limits, or required behind-the-counter placement for diphenhydramine products.

Where does this data come from?

All data in this analysis comes from the FDA Adverse Event Reporting System (FAERS), accessed through the MyfitByte API. FAERS is a publicly available database of adverse event reports submitted to the FDA by healthcare professionals, consumers, and drug manufacturers.

How can I access this data myself?

You can query FAERS data directly through the MyfitByte API. The adverse events endpoint supports filtering by drug name, date range, outcome, patient demographics, and reaction type. Join the waitlist for an API key.


Data source: FDA FAERS (Adverse Event Reporting System), accessed August 2026 via MyfitByte API. Analysis covers all diphenhydramine-linked reports received between January 2018 and December 2025.

Want to run your own analysis on FDA adverse event data? MyfitByte provides structured API access to 2.2M+ FAERS reports with filtering by drug, outcome, demographics, and date. Get early access.

Published on 2026-08-20 · 9 min read

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