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
126028541 12602854 1 I 20160712 20160728 20160728 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00399 AMNEAL 0.00 M Y 0.00000 20160728 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
126028541 12602854 1 PS SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 ONE TABLET, TWO TIMES A DAY U 76899 TABLET
126028541 12602854 2 SS SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 U 76899 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126028541 12602854 1 Infection
126028541 12602854 2 Abscess

Outcome of event

Event ID CASEID OUTC COD
126028541 12602854 OT
126028541 12602854 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126028541 12602854 Chills
126028541 12602854 Condition aggravated
126028541 12602854 Dehydration
126028541 12602854 Heart rate increased
126028541 12602854 Hypotension
126028541 12602854 Irritability
126028541 12602854 Pain
126028541 12602854 Sepsis

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
126028541 12602854 1 20160213 0