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
126128492 12612849 2 F 1998 20160720 20160802 20160804 EXP US-JNJFOC-20160720145 JOHNSON AND JOHNSON LARSON AM. ACETAMINOPHEN-INDUCED ACUTE LIVER FAILURE: RESULTS OF A UNITED STATES MULTICENTER, PROSPECTIVE STUDY. HEPATOLOGY. 2005. 43.00 YR A M Y 94.10000 KG 20160804 MD 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
126128492 12612849 1 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Unknown USED A LOT OF PARACETAMOL OVER LAST 3 YEARS N 0 500 MG UNSPECIFIED
126128492 12612849 2 PS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 Unknown CHRONIC USE (10 DAYS). 6 TO 8, 500 MG/DAY N 19872 31500 MG UNSPECIFIED
126128492 12612849 3 SS KEFLEX CEPHALEXIN 1 Unknown 0 500 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126128492 12612849 1 Product used for unknown indication
126128492 12612849 2 Product used for unknown indication
126128492 12612849 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126128492 12612849 OT
126128492 12612849 DE
126128492 12612849 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126128492 12612849 Acute hepatic failure
126128492 12612849 Arthralgia
126128492 12612849 Brain oedema
126128492 12612849 Chest X-ray abnormal
126128492 12612849 Overdose
126128492 12612849 Sepsis

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
126128492 12612849 1 20020515 0
126128492 12612849 2 199806 0
126128492 12612849 3 19980623 0