The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127770631 12777063 1 I 20100722 20160909 20160923 20160923 EXP US-AMNEAL PHARMACEUTICALS-2016AMN00606 AMNEAL 57.00 YR F Y 52.18000 KG 20160923 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127770631 12777063 1 PS NAPROXEN. NAPROXEN 1 UNK 75927
127770631 12777063 2 C PREDNISONE. PREDNISONE 1 UNK 0
127770631 12777063 3 C FOLIC ACID. FOLIC ACID 1 UNK 0
127770631 12777063 4 C METHOTREXATE. METHOTREXATE 1 UNK 0
127770631 12777063 5 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0
127770631 12777063 6 C DIPHENHYDRAMINE. DIPHENHYDRAMINE 1 UNK 0
127770631 12777063 7 C ACETAMINOPHEN. ACETAMINOPHEN 1 UNK Y 0
127770631 12777063 8 C sultamicillin SULTAMICILLIN 1 UNK 0
127770631 12777063 9 C dolcet 2 UNK Y 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127770631 12777063 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127770631 12777063 Anaemia
127770631 12777063 Cellulitis
127770631 12777063 Pulmonary arterial hypertension

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127770631 12777063 1 20091223 20100628 0
127770631 12777063 2 20091115 0
127770631 12777063 3 20081115 0
127770631 12777063 4 20081115 0
127770631 12777063 5 20081115 0
127770631 12777063 6 20100723 0
127770631 12777063 7 20100723 20100728 0
127770631 12777063 8 20100723 20100804 0
127770631 12777063 9 20100722 20100723 0