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
126766931 12676693 1 I 20160502 20160823 20160823 EXP PT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-116539 RANBAXY 64.00 YR M Y 0.00000 20160823 CN PT PT

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
126766931 12676693 1 SS Vancomycin VANCOMYCIN 1 Unknown UNK Y 0
126766931 12676693 2 PS HYDROCORTISONE. HYDROCORTISONE 1 Unknown UNK U 18726
126766931 12676693 3 SS Adrenaline EPINEPHRINE 1 Unknown UNK Y 0
126766931 12676693 4 SS Amiodarone AMIODARONE 1 Unknown UNK U 0
126766931 12676693 5 SS RANITIDINE. RANITIDINE 1 Unknown UNK U 0
126766931 12676693 6 SS Clemastine CLEMASTINE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126766931 12676693 1 Product used for unknown indication
126766931 12676693 2 Anaphylactic reaction
126766931 12676693 3 Anaphylactic reaction
126766931 12676693 4 Ventricular fibrillation
126766931 12676693 5 Product used for unknown indication
126766931 12676693 6 Anaphylactic reaction

Outcome of event

Event ID CASEID OUTC COD
126766931 12676693 OT
126766931 12676693 LT
126766931 12676693 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126766931 12676693 Anaphylactic shock
126766931 12676693 Bradycardia
126766931 12676693 Cardiac arrest
126766931 12676693 Cardio-respiratory arrest
126766931 12676693 Drug ineffective
126766931 12676693 Hypotension
126766931 12676693 Loss of consciousness
126766931 12676693 Malaise
126766931 12676693 Rash

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

no results found

Therapies reported

no results found