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
109706947 10970694 7 F 2014 20160826 20150331 20160826 EXP US-PFIZER INC-2015104192 PFIZER 58.00 YR M Y 63.00000 KG 20160826 MD 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
109706947 10970694 1 PS RAPAMUNE SIROLIMUS 1 Oral 1 MG, 1X/DAY Y V1N73729 21110 1 MG TABLET QD
109706947 10970694 2 SS RAPAMUNE SIROLIMUS 1 Oral 1 MG, 1X/DAY (WITH MEAL ) Y 21110 1 MG TABLET QD
109706947 10970694 3 SS RAPAMUNE SIROLIMUS 1 Oral 3 MG, 1X/DAY (1MG TABLET, 3 TABLETS BY MOUTH EVERY MORNING) Y 21110 3 MG TABLET QD
109706947 10970694 4 SS TACROLIMUS. TACROLIMUS 1 1 MG, DAILY (1MG, CAPSULES, 9 OR 10 DAILY) Y 0 1 MG
109706947 10970694 5 C CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 36000 IU, 4X/DAY (2 WITH EVERY MEAL SO 8 CAPSULES A DAY) 0 36000 IU CAPSULE QID
109706947 10970694 6 C CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 36000 IU, 2 WITH EACH MEAL 0 36000 IU CAPSULE
109706947 10970694 7 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Oral 1 MG, 3X/DAY TWO IN MORNING AND ONE AT NIGHT 0 1 MG TID
109706947 10970694 8 C LISINOPRIL. LISINOPRIL 1 10 MG, 1X/DAY 0 10 MG QD
109706947 10970694 9 C MYRBETRIQ MIRABEGRON 1 50 MG, 1X/DAY 0 50 MG TABLET QD
109706947 10970694 10 C ASPIRIN. ASPIRIN 1 1 DF, UNK 0 1 DF TABLET
109706947 10970694 11 C FUROSEMIDE. FUROSEMIDE 1 40 MG, 2X/DAY 0 40 MG TABLET BID
109706947 10970694 12 C TAMSULOSIN TAMSULOSIN 1 0.04 MG, UNK 0 .04 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109706947 10970694 1 Pancreatic disorder
109706947 10970694 4 Pancreatic disorder
109706947 10970694 5 Pancreatic disorder
109706947 10970694 6 Diarrhoea
109706947 10970694 8 Renal disorder
109706947 10970694 10 Atrioventricular block
109706947 10970694 11 Renal disorder
109706947 10970694 12 Prostatomegaly

Outcome of event

Event ID CASEID OUTC COD
109706947 10970694 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109706947 10970694 Abdominal pain upper
109706947 10970694 Amnesia
109706947 10970694 Diarrhoea
109706947 10970694 Eating disorder
109706947 10970694 Fatigue
109706947 10970694 Loss of consciousness
109706947 10970694 Malaise
109706947 10970694 Overdose
109706947 10970694 Product use issue
109706947 10970694 Renal impairment
109706947 10970694 Vision blurred

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
109706947 10970694 1 2004 0
109706947 10970694 2 19750904 0
109706947 10970694 3 2004 0
109706947 10970694 4 2004 0