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
8016635 8317521 I 8016635-3 20111213 20111222 20111231 EXP CHPA2011GB018534 SANDOZ,INC. 62 YR F Y 20111231 OT UNITED KINGDOM

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
8016635 1018419945 PS IBUPROFEN 1 TOPICAL UNK, UNK 070733
8016635 1018419956 C TIOPRONIN 1 UNK, UNK
8016635 1018419950 C FLUOXETINE 1 UNK, UNK
8016635 1018419951 C OMEPRAZOLE 1 UNK, UNK
8016635 1018419952 C PREDNISOLONE 1 UNK, UNK
8016635 1018419947 C AMLODIPINE 1 UNK, UNK
8016635 1018419948 C ASPIRIN 1 UNK, UNK
8016635 1018419946 SS LISINOPRIL 1 ORAL UNK, UNK
8016635 1018419953 C ALBUTEROL SULFATE AUTOHALER 1 UNK, UNK
8016635 1018419949 C ACETAMINOPHEN AND CODEINE PHOSPHATE 1 UNK, UNK
8016635 1018419954 C SIMVASTATIN 1 UNK, UNK
8016635 1018419955 C SYMBICORT 1 UNK, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8016635 1018419945 PAIN
8016635 1018419946 HYPERTENSION

Outcome of event

Event ID OUTC COD
8016635 HO

Reactions reported

Event ID PT
8016635 DYSPNOEA
8016635 SWOLLEN TONGUE
8016635 ANGIOEDEMA

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
8016635 1018419945 20111210 20111213 3 DAY
8016635 1018419946 20020101 20111213 3633 DAY