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
7387536 7880612 I 7387536-9 20080922 20110323 20110331 EXP JP-PFIZER INC-2011063718 PFIZERINC 84 YR F Y 20110330 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
7387536 1016142575 PS METHYLPREDNISOLONE SODIUM SUCCINATE 2 INTRAVENOUS DRIP 500MG/DAY 011153
7387536 1016142576 C PREDNISOLONE 2 ORAL UNK
7387536 1016142578 C PREDNISOLONE 2 UNK
7387536 1016142577 C PREDNISOLONE 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
7387536 1016142575 PEMPHIGUS
7387536 1016142576 PEMPHIGUS

Outcome of event

Event ID OUTC COD
7387536 OT

Reactions reported

Event ID PT
7387536 DISSEMINATED INTRAVASCULAR COAGULATION
7387536 PULMONARY ARTERY THROMBOSIS
7387536 VENOUS THROMBOSIS
7387536 SEPSIS

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
7387536 1016142575 20080910 20080912 3 DAY
7387536 1016142576 20080101
7387536 1016142577 20080101