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2013-02-07 - Unknown

499750

Adverse reaction report number 499750
Latest AER version number 0
Market authorization holder AER number ALL1201300534
Initial received date 2013-02-07
Latest received date 2013-02-07
Age N/A
Gender Unknown
Weight N/A
Type of report Spontaneous
Reporter type Pharmacist
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 XRCAPSULE, EXTENDED RELEASESuspectOral1 Dosage forms1 every 1 Day(s) Attention deficit/hyperactivity disorder

Adverse reaction term information

MedDRA version: v.21.1
Adverse reaction terms Reaction duration
Drug effect decreased
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