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
5282289 6276611 I 5282289-2 20070301 20070320 20070331 EXP US-PFIZER INC-2007023768 PFIZER INC M Y 113.4 KG 20070330 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
5282289 1008316837 PS CHANTIX 1 ORAL 021928
5282289 1008316838 SS MOMETASONE FUROATE 1 RESPIRATORY (INHALATION)
5282289 1008316839 C SPIRIVA 1 RESPIRATORY (INHALATION)
5282289 1008316840 C ACETYLSALICYLIC ACID SRT 1
5282289 1008316841 C NOVOLOG 1
5282289 1008316842 C WARFARIN SODIUM 1
5282289 1008316843 C PACERONE 1
5282289 1008316844 C ATENOLOL 1
5282289 1008316845 C LISINOPRIL 1
5282289 1008316846 C SYNTHROID 1
5282289 1008316847 C ZETIA 1
5282289 1008316848 C PRILOSEC 1
5282289 1008316849 C MONTELUKAST SODIUM 1
5282289 1008316850 C NASAREL 1
5282289 1008316851 C KETOROLAC TROMETHAMINE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5282289 1008316837 SMOKING CESSATION THERAPY

Outcome of event

Event ID OUTC COD
5282289 OT

Reactions reported

Event ID PT
5282289 BLOOD GLUCOSE INCREASED
5282289 CANDIDIASIS

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

no results found

Therapies reported

no results found