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
125702882 12570288 2 F 20160627 20160801 20160719 20160805 EXP US-PFIZER INC-2016306349 PFIZER 87.00 YR F Y 0.00000 20160805 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
125702882 12570288 1 PS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Oral UNK 50670
125702882 12570288 2 SS MYCOBUTIN RIFABUTIN 1 Oral 300 MG, DAILY [150 MG; 2 CAPS PER DAY] 50689 300 MG CAPSULE, HARD
125702882 12570288 3 SS ETHAMBUTOL ETHAMBUTOL HYDROCHLORIDE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125702882 12570288 2 Mycobacterium avium complex infection

Outcome of event

Event ID CASEID OUTC COD
125702882 12570288 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125702882 12570288 Asthenia
125702882 12570288 Feeling abnormal
125702882 12570288 Headache
125702882 12570288 Hypoacusis
125702882 12570288 Nausea

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
125702882 12570288 1 20160605 20160627 0
125702882 12570288 2 20160605 20160627 0
125702882 12570288 3 20160605 20160627 0