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
125726981 12572698 1 I 20160706 20160720 20160720 EXP CA-JNJFOC-20160710633 JOHNSON AND JOHNSON 26.00 YR A M Y 0.00000 20160720 OT CA CA

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
125726981 12572698 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Oral U U 19872 TABLET
125726981 12572698 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Oral U U 19872 6500 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125726981 12572698 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125726981 12572698 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125726981 12572698 Abdominal pain
125726981 12572698 Alanine aminotransferase increased
125726981 12572698 Aspartate aminotransferase increased
125726981 12572698 Blood bilirubin increased
125726981 12572698 Blood lactate dehydrogenase increased
125726981 12572698 Blood urea decreased
125726981 12572698 Hepatotoxicity
125726981 12572698 Hyperchloraemia
125726981 12572698 Intentional overdose
125726981 12572698 International normalised ratio increased
125726981 12572698 Thrombocytopenia

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

no results found

Therapies reported

no results found