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
127283121 12728312 1 I 20160829 0 20160907 20160907 DIR US-FDA-349972 FDA-CTU 59.00 YR F N 75.60000 KG 20160907 N 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
127283121 12728312 1 PS PHENERGAN PROMETHAZINE HYDROCHLORIDE 1 Intramuscular Y D 0
127283121 12728312 3 C SOMA CARISOPRODOL 1 0
127283121 12728312 5 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
127283121 12728312 7 C ALPRAZOLAM. ALPRAZOLAM 1 0
127283121 12728312 9 C ADVIL IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127283121 12728312 1 Procedural nausea

Outcome of event

Event ID CASEID OUTC COD
127283121 12728312 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127283121 12728312 Hypoaesthesia
127283121 12728312 Joint swelling
127283121 12728312 Pain
127283121 12728312 Peripheral swelling

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
127283121 12728312 1 20160829 0