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
127247951 12724795 1 I 20150708 20160901 20160908 20160908 EXP ES-AGEMED-143380440 ES-PFIZER INC-2016414415 PFIZER 61.00 YR F Y 0.00000 20160908 MD ES ES

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
127247951 12724795 1 PS CARDURA DOXAZOSIN MESYLATE 1 Oral 16 MG, 1X/DAY 128 MG Y 19668 16 MG MODIFIED-RELEASE TABLET QD
127247951 12724795 2 I LISINOPRIL. LISINOPRIL 1 Oral 20 MG, 1X/DAY 160 MG Y 0 20 MG QD
127247951 12724795 3 I BOI-K ASPARTICO ASPARTIC ACIDPOTASSIUM ASCORBATE 1 Oral 1 DF, 1X/DAY 36 DF Y 0 1 DF QD
127247951 12724795 4 I HYDRAPRES HYDRALAZINE HYDROCHLORIDE 1 Oral 75 MG, 1X/DAY 600 MG Y 0 75 MG QD
127247951 12724795 5 I FUROSEMIDE. FUROSEMIDE 1 Oral 80 MG, 1X/DAY Y 0 80 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127247951 12724795 1 Hypertensive crisis
127247951 12724795 2 Hypertensive crisis
127247951 12724795 4 Hypertensive crisis

Outcome of event

Event ID CASEID OUTC COD
127247951 12724795 OT
127247951 12724795 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127247951 12724795 Acute kidney injury
127247951 12724795 Drug interaction
127247951 12724795 Hyperkalaemia

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
127247951 12724795 1 20150701 20150708 0
127247951 12724795 2 20150701 20150708 0
127247951 12724795 3 20150603 20150708 0
127247951 12724795 4 20150701 20150708 0
127247951 12724795 5 201505 20150708 0