The Safety Rates Drug Report

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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
122153282 12215328 2 F 20160317 20160328 20160720 EXP NL-MYLANLABS-2016M1012807 MYLAN VAN DER SCHAFT J, VAN SCHAIK RHN, VAN DEN BROEK MPH, BRUIJNZEEL-KOOMEN CAFM, DE BRUIN-WELLER MS. INCREASED LIVER ENZYME LEVELS DURING AZATHIOPRINE TREATMENT: BEWARE OF CONCOMITANT USE OF PROTON PUMP INHIBITORS. BR-J-DERMATOL 2015;173(5):1338-1339. 0.00 Y 0.00000 20160720 OT NL NL

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
122153282 12215328 1 PS AZATHIOPRINE. AZATHIOPRINE 1 Unknown STARTED AT 50 MG PER DAY 75568
122153282 12215328 2 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 100 MG PER DAY 75568
122153282 12215328 3 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 150 MG PER DAY 75568
122153282 12215328 4 I PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown 20 MG PER DAY Y U 0
122153282 12215328 5 SS PREDNISOLONE. PREDNISOLONE 1 Oral 20-30 MG PER DAY IN A TAPERING DOSE U U 0
122153282 12215328 6 SS PREDNISOLONE. PREDNISOLONE 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122153282 12215328 1 Dermatitis atopic
122153282 12215328 2 Dyshidrotic eczema
122153282 12215328 4 Gastrointestinal disorder
122153282 12215328 5 Dermatitis atopic
122153282 12215328 6 Dyshidrotic eczema

Outcome of event

Event ID CASEID OUTC COD
122153282 12215328 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122153282 12215328 Drug interaction
122153282 12215328 Gastrointestinal disorder
122153282 12215328 Liver injury
122153282 12215328 Off label use

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

no results found

Therapies reported

no results found