The Safety Rates Drug Report

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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
124913165 12491316 5 F 20140329 20160716 20160623 20160729 EXP IN-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-118839 RANBAXY 74.00 YR M Y 0.00000 20160729 CN IN IN

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
124913165 12491316 1 PS Atorvastatin ATORVASTATIN 1 Unknown UNK Y 76477
124913165 12491316 2 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK U 0
124913165 12491316 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown UNK U 0
124913165 12491316 4 C Olmesartan OLMESARTAN 1 Unknown UNK U 0
124913165 12491316 5 C Pantoprazole PANTOPRAZOLE SODIUM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124913165 12491316 1 Product used for unknown indication
124913165 12491316 2 Product used for unknown indication
124913165 12491316 3 Product used for unknown indication
124913165 12491316 4 Product used for unknown indication
124913165 12491316 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124913165 12491316 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124913165 12491316 Peroneal nerve palsy
124913165 12491316 Rhabdomyolysis
124913165 12491316 Urosepsis

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

no results found

Therapies reported

no results found