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
6250880 7037168 I 6250880-2 20090412 20090415 20090630 PER US-BAUSCH-2009BL001714 BAUSCH + LOMB INCORPORATED 78 YR M Y 20090630 CN UNITED STATES

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
6250880 1011813135 PS ALAWAY 1 OPHTHALMIC A38053 021996
6250880 1011813136 C ADVAIR HFA 1 OROPHARINGEAL
6250880 1011813137 C SPIRIVA 1 OROPHARINGEAL
6250880 1011813138 C METOPROLOL SUCCINATE 1 ORAL
6250880 1011813139 C LISINOPRIL 1 ORAL
6250880 1011813140 C FLOMAX 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6250880 1011813135 EYE PRURITUS
6250880 1011813136 EMPHYSEMA
6250880 1011813137 EMPHYSEMA
6250880 1011813138 HYPERTENSION
6250880 1011813139 HYPERTENSION
6250880 1011813140 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

no results found

Reactions reported

Event ID PT
6250880 EYELID OEDEMA
6250880 SWELLING FACE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6250880 1011813135 20090409 20090412 3 DAY