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
81116112 8111611 2 F 20110103 20121022 20110829 20121029 PER US-BAYER-2011-075062 BAYER 19.00 YR F Y 0.00000 20121029 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
81116112 8111611 1 PS Yasmin 1 D 21098 Film-coated tablet
81116112 8111611 2 SS Yaz 1 D 0 Film-coated tablet
81116112 8111611 3 SS OCELLA 1 D 21098 Film-coated tablet
81116112 8111611 4 C AZATHIOPRINE 1 50 MG A DAY D 0 50 MG
81116112 8111611 5 C Bentryl 2 10 MG, UNK D 0 10 MG TID
81116112 8111611 6 C REMICADE 1 Q 8 WEEK. D 0
81116112 8111611 7 C IMURAN 1 D 0
81116112 8111611 8 C SOLU-MEDROL 1 D 0
81116112 8111611 9 C KEPPRA 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
81116112 8111611 8 Ulcerative colitis
81116112 8111611 9 Focal seizures

Outcome of event

Event ID CASEID OUTC COD
81116112 8111611 HO
81116112 8111611 OT
81116112 8111611 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
81116112 8111611 Cerebrovascular accident
81116112 8111611 Injury
81116112 8111611 Pain
81116112 8111611 Superior sagittal sinus thrombosis
81116112 8111611 Thrombosis

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

no results found

Therapies reported

no results found