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
6662241 7339950 F 6662241-2 20100301 20100324 20100331 EXP US-PFIZER INC-2010029136 PFIZERINC 62 F Y 101 KG 20100331 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
6662241 1013423824 PS CHANTIX 1 ORAL 0.5 MG, 1X/DAY A0417 021928
6662241 1013423825 SS CHANTIX 1 0.5 MG, 2X/DAY A0417 021928
6662241 1013423826 SS CHANTIX 1 1 MG, 2X/DAY 021928
6662241 1013423827 C CYMBALTA 1
6662241 1013423828 C NORCO 1 10 MG, UNK
6662241 1013423829 C ROBAXIN 1 1000 MG, 2X/DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6662241 1013423824 SMOKING CESSATION THERAPY
6662241 1013423827 BIPOLAR DISORDER
6662241 1013423828 BACK PAIN
6662241 1013423829 BACK PAIN

Outcome of event

Event ID OUTC COD
6662241 HO
6662241 OT

Reactions reported

Event ID PT
6662241 ANGER
6662241 ANXIETY
6662241 DRUG DOSE OMISSION
6662241 FEAR
6662241 GASTROINTESTINAL INFECTION
6662241 HOSTILITY
6662241 HYPERSENSITIVITY
6662241 NEOPLASM
6662241 OEDEMA PERIPHERAL
6662241 RASH
6662241 TREATMENT NONCOMPLIANCE

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
6662241 1013423824 20100301 20100301
6662241 1013423825 20100301
6662241 1013423826 20100308 20100323 16 DAY