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
92800215 9280021 5 F 20160704 20130509 20160718 EXP US-RANBAXY-2013US-68648 RANBAXY 53.00 YR M Y 0.00000 20160718 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
92800215 9280021 1 PS Pantoprazole PANTOPRAZOLE SODIUM 1 Oral 40 MG, QD Y 200794 40 MG
92800215 9280021 2 C DILTIAZEM. DILTIAZEM 1 Intravenous (not otherwise specified) UNK U 0
92800215 9280021 3 C HEPARIN HEPARIN SODIUM 1 Intravenous (not otherwise specified) UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92800215 9280021 1 Prophylaxis against gastrointestinal ulcer
92800215 9280021 2 Arrhythmia
92800215 9280021 3 Anticoagulant therapy

Outcome of event

Event ID CASEID OUTC COD
92800215 9280021 LT
92800215 9280021 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
92800215 9280021 Hypomagnesaemia
92800215 9280021 Torsade de pointes
92800215 9280021 Unresponsive to stimuli
92800215 9280021 Ventricular tachycardia

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

no results found

Therapies reported

no results found