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
126139821 12613982 1 I 20160718 0 20160801 20160801 DIR 43.00 YR F N 145.00000 LBS 20160729 N 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
126139821 12613982 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral EVERY 12 HOURS N D 0 Q12H
126139821 12613982 2 C DIVIGEL ESTRADIOL 1 0
126139821 12613982 3 C PROGESTERONE. PROGESTERONE 1 0
126139821 12613982 4 C ZURTEC 2 0
126139821 12613982 5 C FLONASE FLUTICASONE PROPIONATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126139821 12613982 1 Tooth infection

Outcome of event

Event ID CASEID OUTC COD
126139821 12613982 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126139821 12613982 Arthralgia
126139821 12613982 Burning sensation
126139821 12613982 Cardiac flutter
126139821 12613982 Headache
126139821 12613982 Middle insomnia
126139821 12613982 Muscular weakness
126139821 12613982 Pain in extremity
126139821 12613982 Palpitations
126139821 12613982 Paraesthesia
126139821 12613982 Somnolence
126139821 12613982 Tendon 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
126139821 12613982 1 20160714 20160718 0