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
6768591 7406219 F 6768591-3 20100520 20100602 20100614 EXP FR-PFIZER INC-2010066525 PFIZERINC 77 YR M Y 20100614 MD 20100522 FRANCE

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
6768591 1013861997 SS PREDNISONE 1 10 MG, 2X/DAY
6768591 1013861998 SS BLINDED *NO SUBJECT DRUG 2 ORAL 37.5 MG, 1X/DAY 021938
6768591 1013861999 SS BLINDED *PLACEBO 2 ORAL 37.5 MG, 1X/DAY 021938
6768591 1013862000 PS SUNITINIB MALATE 1 ORAL 37.5 MG, 1X/DAY 021938
6768591 1013862001 C RAMIPRIL 2 ORAL UNK
6768591 1013862002 C NICORANDIL 2 ORAL UNK
6768591 1013862003 C ACETYLSALICYLIC ACID 2 ORAL UNK
6768591 1013862004 C BISOPROLOL 2 ORAL UNK
6768591 1013862005 C BECLOMETASONE 2 RESPIRATORY (INHALATION) UNK
6768591 1013862006 C LEUPRORELIN 2 SUBCUTANEOUS 40 MG EVERY 6 MONTHS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6768591 1013861997 PROSTATE CANCER
6768591 1013861998 PROSTATE CANCER
6768591 1013861999 PROSTATE CANCER
6768591 1013862000 PROSTATE CANCER
6768591 1013862001 BLOOD PRESSURE INCREASED
6768591 1013862002 PROPHYLAXIS
6768591 1013862003 PROPHYLAXIS
6768591 1013862004 PROPHYLAXIS
6768591 1013862005 ASTHMA
6768591 1013862006 PROSTATE CANCER

Outcome of event

Event ID OUTC COD
6768591 DE

Reactions reported

Event ID PT
6768591 GENERAL PHYSICAL HEALTH DETERIORATION

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
6768591 1013861997 20100412
6768591 1013861998 20100412 20100520 39 DAY
6768591 1013861999 20100412 20100520 39 DAY
6768591 1013862000 20100412 20100520 39 DAY
6768591 1013862006 20100303