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
127113751 12711375 1 I 20160602 20160829 20160902 20160902 EXP GB-MHRA-EYC 00144298 GB-PFIZER INC-2016408643 PFIZER 42.00 YR F Y 95.00000 KG 20160902 CN GB GB

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
127113751 12711375 1 PS DOXYCYCLINE MONOHYDRATE DOXYCYCLINE 1 500 Y 50006
127113751 12711375 2 SS ERYTHROMYCIN. ERYTHROMYCIN 1 Oral Y 0 250 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127113751 12711375 1 Tooth infection
127113751 12711375 2 Tooth infection

Outcome of event

Event ID CASEID OUTC COD
127113751 12711375 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127113751 12711375 Abdominal discomfort
127113751 12711375 Dizziness
127113751 12711375 Facial pain
127113751 12711375 Head discomfort
127113751 12711375 Headache
127113751 12711375 Hyperhidrosis
127113751 12711375 Pyrexia
127113751 12711375 Renal pain

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
127113751 12711375 1 20160816 20160819 0
127113751 12711375 2 20160601 20160606 0