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
125867981 12586798 1 I 20160107 0 20160722 20160722 DIR 52.00 YR F N 95.00000 LBS 20160721 N PH 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
125867981 12586798 1 PS PHENERGAN PROMETHAZINE HYDROCHLORIDE 1 Intramuscular N D 0 25 MG 1X
125867981 12586798 2 C TRAZODONE HYDROCHLORIDE. TRAZODONE HYDROCHLORIDE 1 0
125867981 12586798 3 C CITALOPRAM HYDROBROMIDE (CELEXA) 2 0
125867981 12586798 4 C CHLORZOXAZONE (PARAFON FORTE DSC) 2 0
125867981 12586798 5 C ACETAMINOPHENHYDROCODONE BITARTRATE ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
125867981 12586798 6 C PROMETHAZINE HCL PROMETHAZINE HYDROCHLORIDE 1 0
125867981 12586798 7 C PANTOPRAZOLE SODIUM. PANTOPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125867981 12586798 1 Nausea

Outcome of event

Event ID CASEID OUTC COD
125867981 12586798 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125867981 12586798 Asthenia
125867981 12586798 Contusion
125867981 12586798 Hypoaesthesia
125867981 12586798 Injection site abscess
125867981 12586798 Injection site hypoaesthesia
125867981 12586798 Musculoskeletal pain
125867981 12586798 Neuropathy peripheral
125867981 12586798 Osteomyelitis
125867981 12586798 Pain in extremity
125867981 12586798 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
125867981 12586798 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125867981 12586798 1 20160107 20160107 0