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
124924622 12492462 2 F 2016 20160714 20160623 20160715 EXP PH-009507513-1606PHL010515 MERCK 55.00 YR F Y 0.00000 20160715 CN PH PH

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
124924622 12492462 1 PS DIPROSPAN BETAMETHASONE DIPROPIONATEBETAMETHASONE SODIUM PHOSPHATE 1 UNK Y 19555 INJECTION
124924622 12492462 2 SS LIDOCAINE. LIDOCAINE 1 STRENGTH: 0.2 SOLUTION (1CC) Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124924622 12492462 1 Trigger finger
124924622 12492462 2 Trigger finger

Outcome of event

Event ID CASEID OUTC COD
124924622 12492462 HO
124924622 12492462 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124924622 12492462 Dyspnoea
124924622 12492462 Erythema
124924622 12492462 General anaesthesia
124924622 12492462 Pruritus
124924622 12492462 Surgery
124924622 12492462 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
124924622 12492462 1 20160620 20160620 0
124924622 12492462 2 20160620 20160620 0