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
105665523 10566552 3 F 2007 20160624 20141105 20160706 EXP PT-MYLANLABS-2014M1009098 MYLAN JOSE PEDRO ALMEIDA, ANABELA LOPES, MANUEL PEREIRA BARBOSA. REVISTA PORTUGUESA DE IMUNOALERGOLOGIA. OFFICIAL JOURNAL OF THE PORTUGUESE SOCIETY OF ALLERGOLOGY AND CLINICAL IMMUNOLOG. 2013;21:5 - 43 0.00 Y 0.00000 20160706 OT PT PT

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
105665523 10566552 1 SS OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK U 0
105665523 10566552 2 SS OMEPRAZOLE. OMEPRAZOLE 1 40 MG, QD U 0 40 MG QD
105665523 10566552 3 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0
105665523 10566552 4 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral UNK U 0
105665523 10566552 5 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0
105665523 10566552 6 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0
105665523 10566552 7 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0
105665523 10566552 8 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 40 MG, UNK U 0 40 MG QD
105665523 10566552 9 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0
105665523 10566552 10 SS OMEPRAZOLE. OMEPRAZOLE 1 U 0
105665523 10566552 11 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral U 90763
105665523 10566552 12 SS LANSOPRAZOLE. LANSOPRAZOLE 1 U 90763
105665523 10566552 13 SS LANSOPRAZOLE. LANSOPRAZOLE 1 U 90763
105665523 10566552 14 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral U 0
105665523 10566552 15 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 U 0
105665523 10566552 16 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 U 0
105665523 10566552 17 SS ESOMEPRAZOLE ESOMEPRAZOLE 1 Oral U 0
105665523 10566552 18 SS RABEPRAZOLE RABEPRAZOLE 1 Oral U 0
105665523 10566552 19 SS RABEPRAZOLE RABEPRAZOLE 1 U 0
105665523 10566552 20 SS RABEPRAZOLE RABEPRAZOLE 1 U 0
105665523 10566552 21 C DESLORATADINE. DESLORATADINE 1 Unknown 5 MG, QD U 0 5 MG QD
105665523 10566552 22 C ACETYLSALICYLATE LYSINE ASPIRIN DL-LYSINE 1 Intravenous (not otherwise specified) UNK U 0
105665523 10566552 23 C IBUPROFEN. IBUPROFEN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105665523 10566552 1 Gastrooesophageal reflux disease
105665523 10566552 2 Prophylaxis
105665523 10566552 3 Influenza
105665523 10566552 5 Gastrooesophageal reflux disease
105665523 10566552 6 Influenza
105665523 10566552 7 Prophylaxis
105665523 10566552 9 Gastrooesophageal reflux disease
105665523 10566552 10 Prophylaxis
105665523 10566552 12 Gastrooesophageal reflux disease
105665523 10566552 13 Prophylaxis
105665523 10566552 15 Gastrooesophageal reflux disease
105665523 10566552 16 Prophylaxis
105665523 10566552 19 Gastrooesophageal reflux disease
105665523 10566552 20 Prophylaxis
105665523 10566552 21 Product used for unknown indication
105665523 10566552 22 Product used for unknown indication
105665523 10566552 23 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105665523 10566552 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105665523 10566552 Angioedema
105665523 10566552 Drug hypersensitivity
105665523 10566552 Erythema

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
105665523 10566552 1 2007 0
105665523 10566552 22 2007 0