The Safety Rates Drug Report

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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
5701501 6817974 I 5701501-6 20080101 20080320 20080407 EXP 530#6#2008-00011 SCHWARZ PHARMA DEUTSCHLAND GMBH 83 YR M N 20080402 MD GERMANY

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
5701501 1009771744 PS NEURO-PATCH-DOSE (ROTIGOTINE) 2 TRANSDERMAL 2 MG/24H (2 MG/24H 1 IN 1 DAY (S)) TRANSDERMAL, 4 MG/24H (4 MG/24 H 1 IN 1 DAY (S)) TRANSDERMAL D D 21829
5701501 1009804001 SS CARBIDOPA AND LEVODOPA 1 ORAL 3 X 200/50 MG PER DAY ORAL
5701501 1009804004 SS CARBIDOPA AND LEVODOPA 1 ORAL 3 X 100/25 MG PER DAY ORAL
5701501 1009804009 C ACETYLSALICYLIC ACID SRT 1
5701501 1009804020 C INSULIN HUMAN, ISOPHANE 2 21829
5701501 1009804024 C INSULIN ASPART 1
5701501 1009804025 C METOPROLOL TARTRATE 1
5701501 1009804032 C OXYCODONE HCL 1
5701501 1009804036 C TORSEMIDE 1
5701501 1009804038 C TRIMPRAMINE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5701501 1009771744 PARKINSON'S DISEASE
5701501 1009804001 PARKINSON'S DISEASE
5701501 1009804004 PARKINSON'S DISEASE

Outcome of event

Event ID OUTC COD
5701501 DE
5701501 HO

Reactions reported

Event ID PT
5701501 PNEUMONIA

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

Event ID RPSR COD
5701501 FGN
5701501 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5701501 1009771744 20071023 20071025
5701501 1009771744 20071026
5701501 1009804001 20060601 20071025 17 MON
5701501 1009804004 20071026