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
127685721 12768572 1 I 20160826 20160914 20160921 20160921 EXP FR-PFIZER INC-2016432739 PFIZER 54.00 YR M Y 0.00000 20160921 OT FR FR

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
127685721 12768572 1 PS ALDACTONE SPIRONOLACTONE 1 Oral 12151 TABLET
127685721 12768572 2 SS TAHOR ATORVASTATIN CALCIUM 1 Oral Y 20702
127685721 12768572 3 SS IRBESARTAN. IRBESARTAN 1 0
127685721 12768572 4 C PREVISCAN /00261401/ PENTOXIFYLLINE 1 0
127685721 12768572 5 C CORDARONE AMIODARONE HYDROCHLORIDE 1 0
127685721 12768572 6 C CARDENSIEL BISOPROLOL FUMARATE 1 0
127685721 12768572 7 C KARDEGIC ASPIRIN LYSINE 1 0
127685721 12768572 8 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127685721 12768572 1 Hypertension
127685721 12768572 2 Hypercholesterolaemia
127685721 12768572 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127685721 12768572 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127685721 12768572 Acute kidney injury
127685721 12768572 Anuria
127685721 12768572 Hyperthermia
127685721 12768572 Malaise
127685721 12768572 Myalgia
127685721 12768572 Rhabdomyolysis

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

no results found

Therapies reported

no results found