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
6024914 6870778 I 6024914-4 20081123 20081222 20081231 EXP GB-PFIZER INC-2008159160 PFIZERINC Y 20081231 OT UNITED KINGDOM

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
6024914 1010941290 PS CHAMPIX 2 ORAL 0.5 MG, 2X/DAY 21928
6024914 1010941291 C SALBUTAMOL SULFATE 2 UNK
6024914 1010941292 C SPIRIVA 1 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6024914 1010941290 SMOKING CESSATION THERAPY
6024914 1010941291 CHRONIC OBSTRUCTIVE PULMONARY DISEASE
6024914 1010941292 CHRONIC OBSTRUCTIVE PULMONARY DISEASE

Outcome of event

Event ID OUTC COD
6024914 OT

Reactions reported

Event ID PT
6024914 ABDOMINAL DISTENSION
6024914 CRYING
6024914 DEPRESSED MOOD
6024914 DRY MOUTH
6024914 FEELING COLD

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
6024914 1010941290 20081121 20081125 5 DAY
6024914 1010941291 20071120
6024914 1010941292 20071016