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
8623745 8503268 F 8623745-6 20120304 20120820 20120827 EXP JP-PFIZER INC-2012088261 PFIZERINC 38 YR F Y 72 KG 20120827 MD JAPAN

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
8623745 1020671044 PS ZOSYN 1 INTRAVENOUS DRIP UNK 050684
8623745 1020671047 C METFORMIN HCL 1 ORAL 250 MG, 1X/DAY
8623745 1020671048 C MUCODYNE 2 ORAL 1500 MG, 1X/DAY
8623745 1020671045 C HUMALOG 1 SUBCUTANEOUS 27 IU, 1X/DAY
8623745 1020671046 C LANTUS 1 SUBCUTANEOUS 16 IU, 1X/DAY
8623745 1020671049 C ASTOMIN 2 ORAL 30 MG, 1X/DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
8623745 1020671044 PYELONEPHRITIS
8623745 1020671047 DIABETES MELLITUS
8623745 1020671048 PRODUCTIVE COUGH
8623745 1020671045 DIABETES MELLITUS
8623745 1020671046 DIABETES MELLITUS
8623745 1020671049 ANTITUSSIVE THERAPY

Outcome of event

Event ID OUTC COD
8623745 HO

Reactions reported

Event ID PT
8623745 INTERSTITIAL LUNG DISEASE

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
8623745 1020671044 20120228 20120304 6 DAY
8623745 1020671048 20120228 20120314 16 DAY
8623745 1020671049 20120228 20120314 16 DAY