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
127314561 12731456 1 I 20160829 20160912 20160912 EXP NO-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-123724 RANBAXY 82.00 YR M Y 0.00000 20160912 OT NO NO

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
127314561 12731456 1 PS Paracet ACETAMINOPHEN 1 Unknown UNK U 78569
127314561 12731456 2 SS Ciproxin CIPROFLOXACIN 1 Unknown U 0
127314561 12731456 3 SS FLAGYL METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127314561 12731456 1 Product used for unknown indication
127314561 12731456 2 Product used for unknown indication
127314561 12731456 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127314561 12731456 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127314561 12731456 Hepatocellular injury
127314561 12731456 Jaundice

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

no results found

Therapies reported

no results found