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
126495671 12649567 1 I 201607 20160805 20160812 20160812 EXP IT-MINISAL02-370372 IT-MYLANLABS-2016M1033303 MYLAN 0.00 Y 0.00000 20160812 MD IT IT

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
126495671 12649567 1 PS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 20 MG, QD Y 90970 20 MG QD
126495671 12649567 2 C PIPERACILLIN AND TAZOBACTAM PIPERACILLIN SODIUMTAZOBACTAM SODIUM 1 0
126495671 12649567 3 C CEFAZOLIN CEFAZOLIN 1 0
126495671 12649567 4 C RIFAMPICIN RIFAMPIN 1 0
126495671 12649567 5 C CIPROFLOXACIN. CIPROFLOXACIN 1 0
126495671 12649567 6 C TIGECYCLINE. TIGECYCLINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126495671 12649567 1 Dyspepsia
126495671 12649567 2 Product used for unknown indication
126495671 12649567 3 Product used for unknown indication
126495671 12649567 4 Product used for unknown indication
126495671 12649567 5 Product used for unknown indication
126495671 12649567 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126495671 12649567 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126495671 12649567 Anaemia
126495671 12649567 Diverticulum intestinal
126495671 12649567 Hepatitis cholestatic
126495671 12649567 Interstitial lung disease
126495671 12649567 Thrombocytopenia

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
126495671 12649567 1 20160604 20160704 0