The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
88604817 8860481 7 F 201102 20160805 20121025 20160818 EXP US-JNJFOC-20121011489 JOHNSON AND JOHNSON 40.66 YR A F Y 70.31000 KG 20160818 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
88604817 8860481 1 PS TYLENOL ACETAMINOPHEN 1 Oral N 19872 UNSPECIFIED
88604817 8860481 2 SS TYLENOL ACETAMINOPHEN 1 Oral N 19872 UNSPECIFIED
88604817 8860481 3 SS TYLENOL PM ACETAMINOPHENDIPHENHYDRAMINE 1 Oral N 999999 CAPLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88604817 8860481 1 Sleep disorder therapy
88604817 8860481 2 Pain
88604817 8860481 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
88604817 8860481 DE
88604817 8860481 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
88604817 8860481 Acute hepatic failure
88604817 8860481 Acute kidney injury
88604817 8860481 Brain death
88604817 8860481 Coagulopathy
88604817 8860481 Coma
88604817 8860481 Hepatorenal syndrome
88604817 8860481 Intentional overdose
88604817 8860481 Metabolic acidosis
88604817 8860481 Renal failure
88604817 8860481 Respiratory failure
88604817 8860481 Sepsis
88604817 8860481 Shock
88604817 8860481 Toxicity to various agents

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
88604817 8860481 1 20110207 20110208 0
88604817 8860481 2 20110207 20110208 0
88604817 8860481 3 201102 0