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2017-09-27 - Unknown

901504795

Adverse reaction report number 901504795
Latest AER version number 0
Market authorization holder AER number CA201722992
Initial received date 2017-09-27
Latest received date 2017-09-27
Age N/A
Gender Unknown
Weight N/A
Type of report Spontaneous
Reporter type Consumer Or Other Non Health Professional
Source of report MAH
Report outcome Unknown
Serious report? No

Product information

Product description Dosage form Health product role Route of administration Dose Frequency Therapy duration Indication(s)
ADDERALL XRCAPSULESuspectUnknown15 Milligram1 every 1 Day(s) Product used for unknown indication
ADDERALL XRCAPSULESuspectUnknown25 Milligram1 every 1 Day(s) Product used for unknown indication
ADDERALL XRCAPSULESuspectUnknown30 Milligram1 every 1 Day(s) Product used for unknown indication
ADDERALL XRCAPSULE, EXTENDED RELEASESuspectUnknown15 Milligram1 every 1 Day(s) Product used for unknown indication
BENADRYL /00000402/Concomitant Product used for unknown indication

Adverse reaction term information

MedDRA version: v.21.1
Adverse reaction terms Reaction duration
Drug effect decreased
Intentional product misuse
Rash pruritic
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