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
127290851 12729085 1 I 20160602 20160829 20160909 20160909 EXP GB-MHRA-EYC 00144298 GB-TEVA-689310ACC TEVA 42.00 YR F Y 95.00000 KG 20160909 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
127290851 12729085 1 PS DOXYCYCLINE. DOXYCYCLINE 1 500 Y U 62497
127290851 12729085 2 SS ERYTHROMYCIN. ERYTHROMYCIN 1 Oral Y U 62999 250 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127290851 12729085 1 Tooth infection
127290851 12729085 2 Tooth infection

Outcome of event

Event ID CASEID OUTC COD
127290851 12729085 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127290851 12729085 Abdominal discomfort
127290851 12729085 Dizziness
127290851 12729085 Facial pain
127290851 12729085 Head discomfort
127290851 12729085 Headache
127290851 12729085 Hyperhidrosis
127290851 12729085 Pyrexia
127290851 12729085 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
127290851 12729085 1 20160816 20160819 0
127290851 12729085 2 20160601 20160606 0