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
124054372 12405437 2 F 20160810 20160525 20160817 EXP JP-ABBVIE-16P-087-1637123-00 ABBVIE 51.00 YR F Y 0.00000 20160817 OT JP JP

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
124054372 12405437 1 PS CLARITH CLARITHROMYCIN 1 Oral U UNKNOWN 50662
124054372 12405437 2 SS TEGRETOL CARBAMAZEPINE 1 Oral U UNKNOWN 0
124054372 12405437 3 SS PL ACETAMINOPHENCAFFEINEPROMETHAZINESALICYLAMIDE 1 Oral U UNKNOWN 0
124054372 12405437 4 SS GASTER FAMOTIDINE 1 Oral U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124054372 12405437 1 Product used for unknown indication
124054372 12405437 2 Product used for unknown indication
124054372 12405437 3 Product used for unknown indication
124054372 12405437 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124054372 12405437 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124054372 12405437 Erythema multiforme

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
124054372 12405437 1 201504 201504 0