FDA Recalls & Drug Adverse Events Data, $1/1K, No Login
Pricing
from $0.70 / 1,000 fda records
Get FDA drug recalls, medical device recalls and drug adverse event reports from the official openFDA API. Filter by search term, date and recall class. One row per recall or report, or event counts by reaction, drug or country. $1 per 1,000 records. Unofficial, not affiliated with the FDA.
mode
Optional
drug_recalls, device_recalls, adverse_event_counts or adverse_event_reports.
query
Optional
The search term, if any.
recallNumber
Optional
Recalls: FDA recall number.
eventId
Optional
Recalls: FDA recall event ID (one event can cover several products).
classification
Optional
Recalls: Class I, II or III.
recallStatus
Optional
Recalls: Ongoing, Completed or Terminated.
productType
Optional
Recalls: Drugs or Devices.
productDescription
Optional
Recalls: the recalled product.
reasonForRecall
Optional
Recalls: why the product was recalled.
productQuantity
Optional
Recalls: quantity recalled.
codeInfo
Optional
Recalls: lot numbers and codes affected.
recallingFirm
Optional
Recalls: the company recalling the product.
city
Optional
Recalls: firm city.
state
Optional
Recalls: firm state.
country
Optional
Recalls: firm country.
voluntaryMandated
Optional
Recalls: voluntary (firm initiated) or FDA mandated.
distributionPattern
Optional
Recalls: where the product was distributed.
recallInitiationDate
Optional
Recalls: date the recall started (YYYY-MM-DD).
reportDate
Optional
Recalls: date of the FDA enforcement report.
terminationDate
Optional
Recalls: date the recall was terminated, if it was.
brandNames
Optional
Recalls: brand names linked by openFDA.
genericNames
Optional
Recalls: generic names linked by openFDA.
reportId
Optional
Adverse event reports: safety report ID.
receivedDate
Optional
Adverse event reports: date FDA received the report.
serious
Optional
Adverse event reports: true when the event was serious.
seriousnessReasons
Optional
Adverse event reports: death, life-threatening, hospitalization, disability, congenital anomaly or other serious.
reportCountry
Optional
Adverse event reports: country where the event occurred.
reporterType
Optional
Adverse event reports: physician, pharmacist, consumer and so on.
drugs
Optional
Adverse event reports: drug names as reported.
activeSubstances
Optional
Adverse event reports: active substances.
reactions
Optional
Adverse event reports: reactions (MedDRA terms).
countBy
Optional
Adverse event counts: what is counted.
term
Optional
Adverse event counts: the reaction, drug, country or other value.
count
Optional
Adverse event counts: number of reports.
status
Required
ok (charged), or a free status: no_results, invalid_query, rate_limited, api_error or invalid_input.
error
Optional
Why the row is not ok.
charged
Required
True when this row was charged.
credit
Optional
Data credit line required by openFDA: Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
