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2018-11-08 - Female - 59 Years old

720027

Adverse reaction report number 720027
Latest AER version number 0
Market authorization holder AER number 630947
Initial received date 2018-11-08
Latest received date 2018-11-08
Age 59 Years
Gender Female
Weight N/A
Type of report Spontaneous
Reporter type Physician
Source of report MAH
Report outcome Recovered/resolved
Serious report? Yes

Reason for seriousness

Death
Disability
Cogenital anomaly
Life threateting
Hospitalization Yes
Other medically important Yes

Product information

Product description Dosage form Health product role Route of administration Dose Frequency Therapy duration Indication(s)
CRESTORTABLETSuspectUnknown Product used for unknown indication
METFORMINSuspectUnknown Product used for unknown indication
OZEMPICSOLUTION SUBCUTANEOUSSuspectUnknown0.25 Milligram1 every 1 Day(s)1 Week(s)Product used for unknown indication
OZEMPICSOLUTION SUBCUTANEOUSSuspectUnknown0.5 Milligram1 every 1 Day(s) Product used for unknown indication
RAMIPRILTABLETSuspectUnknown Product used for unknown indication

Adverse reaction term information

MedDRA version: v.21.1
Adverse reaction terms Reaction duration
Alanine aminotransferase increased
Aspartate aminotransferase increased
Blood creatine phosphokinase increased
Malaise
Weight decreased
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