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
125733541 12573354 1 I 20160706 20160720 20160720 EXP CA-JNJFOC-20160710646 JOHNSON AND JOHNSON 45.00 YR A F Y 60.00000 KG 20160720 PH 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
125733541 12573354 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 TABLET
125733541 12573354 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 5200 MG TABLET QD
125733541 12573354 3 C ENOXAPARIN ENOXAPARIN 1 Unknown 0 INJECTION
125733541 12573354 4 C WARFARIN WARFARIN 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125733541 12573354 2 Product used for unknown indication
125733541 12573354 3 Product used for unknown indication
125733541 12573354 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125733541 12573354 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125733541 12573354 Alanine aminotransferase increased
125733541 12573354 Aspartate aminotransferase increased
125733541 12573354 Blood lactate dehydrogenase increased
125733541 12573354 Hypokalaemia
125733541 12573354 Metabolic acidosis
125733541 12573354 Nausea
125733541 12573354 Overdose
125733541 12573354 Renal failure
125733541 12573354 Vomiting

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

no results found

Therapies reported

no results found