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
1004683912 10046839 12 F 20100818 20160916 20140331 20160929 EXP US-JNJFOC-20140312018 JOHNSON AND JOHNSON 30.07 YR A F Y 58.97000 KG 20160929 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
1004683912 10046839 1 PS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral Y N 19872 TABLET
1004683912 10046839 2 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Oral Y N 19872 1000 MG TABLET Q4H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1004683912 10046839 2 Toothache

Outcome of event

Event ID CASEID OUTC COD
1004683912 10046839 OT
1004683912 10046839 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
1004683912 10046839 Acute hepatic failure
1004683912 10046839 Acute kidney injury
1004683912 10046839 Anaemia
1004683912 10046839 Coagulopathy
1004683912 10046839 Lactic acidosis
1004683912 10046839 Overdose
1004683912 10046839 Peritoneal haemorrhage
1004683912 10046839 Thrombocytopenia
1004683912 10046839 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
1004683912 10046839 2 20100817 20100818 0