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
127093521 12709352 1 I 20160815 0 20160901 20160901 DIR 65.00 YR F N 170.00000 LBS 20160831 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
127093521 12709352 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Sublingual Y D 0 Q12H
127093521 12709352 3 C BENICAR OLMESARTAN MEDOXOMIL 1 0
127093521 12709352 5 C ATIVAN LORAZEPAM 1 0
127093521 12709352 7 C PHRENILIN ACETAMINOPHENBUTALBITAL 1 0
127093521 12709352 9 C VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127093521 12709352 1 Pain

Outcome of event

Event ID CASEID OUTC COD
127093521 12709352 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127093521 12709352 Confusional state
127093521 12709352 Dizziness
127093521 12709352 Dysgeusia
127093521 12709352 Hallucination
127093521 12709352 Hyperacusis
127093521 12709352 Hyperhidrosis
127093521 12709352 Movement disorder
127093521 12709352 Nausea
127093521 12709352 Vomiting

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
127093521 12709352 1 20160815 20160815 0