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
111350292 11135029 2 F 20150511 20150525 20160722 PER US-SUN PHARMACEUTICAL INDUSTRIES LTD-2015US-97420 RANBAXY 0.00 F Y 0.00000 20160722 CN 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
111350292 11135029 1 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown UNK U 0 TABLET
111350292 11135029 2 SS Morphine MORPHINE 1 Unknown UNK U 0
111350292 11135029 3 SS DOXYCYCLINE. DOXYCYCLINE 1 Unknown UNK U 0
111350292 11135029 4 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown UNK U 75747
111350292 11135029 5 SS LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111350292 11135029 1 Product used for unknown indication
111350292 11135029 2 Product used for unknown indication
111350292 11135029 3 Product used for unknown indication
111350292 11135029 4 Product used for unknown indication
111350292 11135029 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111350292 11135029 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111350292 11135029 Drug hypersensitivity

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

no results found

Therapies reported

no results found