The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
4787283 5824737 F 2 4787283-3 20050422 20050914 20050930 EXP CAO05000699 PROCTER + GAMBLE REGULATORY AFFAIRS 77 YR M N 20050928 CANADA

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
4787283 1006480328 PS METAMUCIL-2 1 ORAL 1 TBSP, 3/DAY FOR 4 DAYS, ORAL D D 4240ARA1 20071201
4787283 1006501563 C PLAVIX 1
4787283 1006501564 C ASPIRIN 1
4787283 1006501565 C NORVASC 1
4787283 1006501566 C COZAAR 1
4787283 1006501567 C LASIX (FUROSEMIDE SODIUM, FUROSEMIDE) 2
4787283 1006501568 C ELTROXIN (LEVOTHYROXINE SODIUM) 2
4787283 1006501569 C ZANTAC 1
4787283 1006501570 C LOPRESSOR 1
4787283 1006501572 C LIPITOR 1
4787283 1006501573 C COLIC 2
4787283 1006501602 C HYTRIN 1
4787283 1006501618 C RAVOTRIL (CLONAZEPAM) 2
4787283 1006501672 C TIAPROFENIC ACID (TIAPROFENIC ACID) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4787283 1006480328 PROPHYLAXIS

Outcome of event

Event ID OUTC COD
4787283 HO

Reactions reported

Event ID PT
4787283 ABDOMINAL DISTENSION
4787283 DIARRHOEA
4787283 MALAISE
4787283 NAUSEA
4787283 NO REACTION ON PREVIOUS EXPOSURE TO DRUG
4787283 PHARMACEUTICAL PRODUCT COMPLAINT
4787283 VOMITING

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

Event ID RPSR COD
4787283 CSM
4787283 FGN
4787283 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4787283 1006480328 20050422 20050513