The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6810137 7448874 I 6810137-5 20070101 20100622 20100630 EXP NL-WATSON-2010-08502 WATSON 47 YR M Y 20100630 OT NETHERLANDS

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6810137 1014006339 PS PREDNISOLONE (WATSON LABORATORIES) 2 10 MG, DAILY UNCONFIRMED 80354
6810137 1014006340 SS AZATHIOPRINE 1 175 MG, DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6810137 1014006339 PROPHYLAXIS AGAINST TRANSPLANT REJECTION
6810137 1014006340 PROPHYLAXIS AGAINST TRANSPLANT REJECTION

Outcome of event

Event ID OUTC COD
6810137 OT

Reactions reported

Event ID PT
6810137 SQUAMOUS CELL CARCINOMA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6810137 1014006339 9125 DAY
6810137 1014006340 9125 DAY