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
126292851 12629285 1 I 2016 20160725 20160808 20160808 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-121744 RANBAXY 54.00 YR F Y 84.35000 KG 20160808 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
126292851 12629285 1 PS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown UNK 18374
126292851 12629285 2 C TRAMADOL. TRAMADOL 1 Unknown UNK 0
126292851 12629285 3 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown UNK 0
126292851 12629285 4 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 Unknown UNK 0
126292851 12629285 5 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK 0
126292851 12629285 6 C SINGULAIR MONTELUKAST SODIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126292851 12629285 1 Injection site reaction
126292851 12629285 2 Product used for unknown indication
126292851 12629285 3 Product used for unknown indication
126292851 12629285 4 Product used for unknown indication
126292851 12629285 5 Product used for unknown indication
126292851 12629285 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126292851 12629285 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126292851 12629285 Drug ineffective
126292851 12629285 Urticaria

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
126292851 12629285 1 20160505 20160512 0