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Aralen (Chloroquine) - Disability - Suspected Cause - Side Effect Reports

 
 



Index of reports > Disability (2)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Aralen (Chloroquine) disability. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Aralen side effects in 53 year old female

Reported by a consumer/non-health professional from Mexico on 2012-04-11

Patient: 53 year old female, weighing 71.0 kg (156.2 pounds)

Reactions: Cataract, Anaemia, Vision Blurred

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Aralen
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2008-01-01

Deflazacort
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2008-01-01

Arava
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2008-01-01

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2007-01-01



Possible Aralen side effects in 53 year old female

Reported by a consumer/non-health professional from Mexico on 2012-03-23

Patient: 53 year old female, weighing 71.0 kg (156.2 pounds)

Reactions: Cataract, Anaemia, Vision Blurred

Adverse event resulted in: disablity

Drug(s) suspected as cause:
Deflazacort
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2008-01-01

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2007-01-01

Arava
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2008-01-01

Aralen
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2008-01-01

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