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
127770161 12777016 1 I 20110220 20160909 20160923 20160923 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00620 AMNEAL 68.00 YR F Y 101.59000 KG 20160923 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
127770161 12777016 1 PS NAPROXEN. NAPROXEN 1 UNK N 75927
127770161 12777016 2 C byetta insulin 2 UNK U 0
127770161 12777016 3 C XYZAL LEVOCETIRIZINE DIHYDROCHLORIDE 1 UNK U 0
127770161 12777016 4 C LISINOPRIL. LISINOPRIL 1 UNK U 0
127770161 12777016 5 C baby aspirin ASPIRIN 1 UNK U 0
127770161 12777016 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 UNK U 0
127770161 12777016 7 C SYNTHROID LEVOTHYROXINE SODIUM 1 UNK U 0
127770161 12777016 8 C SIMVASTATIN. SIMVASTATIN 1 UNK 0
127770161 12777016 9 C ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 UNK 0
127770161 12777016 10 C pantoprazole PANTOPRAZOLE SODIUM 1 U 0
127770161 12777016 11 C CARDIZEM CD DILTIAZEM HYDROCHLORIDE 1 U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127770161 12777016 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127770161 12777016 Coronary artery disease

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
127770161 12777016 1 20080805 20120220 0
127770161 12777016 2 20100411 0
127770161 12777016 3 20091015 0
127770161 12777016 4 20110830 0
127770161 12777016 5 20110914 0
127770161 12777016 6 20090201 0
127770161 12777016 7 1968 0
127770161 12777016 8 20120206 20120309 0
127770161 12777016 9 20120119 0