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
73518984 7351898 4 F 20131219 20100412 20131231 EXP US-BAYER-201018765NA BAYER 25.00 YR F Y 50.00000 KG 20131231 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
73518984 7351898 1 PS Yaz 1 ORAL UNK UNK, UNK D UNKNOWN 21676 FILM-COATED TABLET
73518984 7351898 2 C IMITREX 1 UNK D 0
73518984 7351898 3 C MIGRANAL 1 D 0
73518984 7351898 4 C Advil 1 D 0
73518984 7351898 5 C EFFEXOR 1 UNK D 0
73518984 7351898 6 C LORATAB 1 UNK D 0
73518984 7351898 7 C ZANTAC 1 UNK D 0
73518984 7351898 8 C SUBLIMAZE 1 UNK D 0
73518984 7351898 9 C VICODIN 1 ORAL UNK D 0
73518984 7351898 10 C LITHIUM CARBONATE 1 UNK D 0
73518984 7351898 11 C PROZAC 1 UNK D 0
73518984 7351898 12 C LAMICTAL 1 UNK D 0
73518984 7351898 13 C TRAZODONE 1 UNK D 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
73518984 7351898 HO
73518984 7351898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
73518984 7351898 Cholecystitis chronic
73518984 7351898 Gallbladder injury

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
73518984 7351898 1 2007 2008 0
73518984 7351898 2 200503 0
73518984 7351898 5 200801 0
73518984 7351898 6 200801 0
73518984 7351898 7 200801 0
73518984 7351898 8 200801 0
73518984 7351898 9 200711 0
73518984 7351898 10 200702 0
73518984 7351898 11 200702 0
73518984 7351898 12 200503 0
73518984 7351898 13 200503 0