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strattera side effects liver
The majority of reported Strattera overdose effects were moderate. They included tachycardia and dry mouth, convulsions, hyperactivity, behavioral disorders, drowsiness or agitation, stomach upset, mydriasis (an excessive dilation of the pupil), blurred vision, drowsiness, and fast heartbeat.
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This medication cannot be co-administered with MAO inhibitors, a break between the last MAO inhibitors intake such as Nardil (phenelzine sulfate) and Parnate (tranylcypromine sulfate) and administration of Strattera should be at least 14 days long. Fluoxetine (Prozac), paroxetine (Paxil), quinidine, may incrase blood levels of Strattera due to inhibition of the liver enzyme that eliminates atomoxetine from the body. Inform your doctor about all medications and herbal products you use including albuterol (Proventil, Ventolin), bupropion (Wellbutrin, Zyban), cimetidine (Tagamet), amiodarone (Cordarone, Pacerone), celecoxib (Celebrex), methadone (Methadose, Dolophine), quinidine (Quinidex, Cardioquin, Quinaglute), doxorubicin (Adriamycin), ranitidine (Zantac), terbinafine (Lamisil), metoclopramide (Reglan), ritonavir (Norvir).
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Take it once or twice daily with or without food. Take the capsules whole, do not crush them and sprinkle on food. If Strattera should be canceled, it does not require a gradual reduction of the dose. The recommended initial dose in children, adolescents and adults with body weight over 70 kg is 40 mg. It should be increased to a therapeutic daily dose of 80 mg not earlier than in three days. If the symptoms do not improve the maximal daily dose of Strattera may be increased to maximal daily dose of 120 mg not earlier than 2-4 weeks after start of the treatment. Take exactly as prescribed by your doctor, do not take more of this medication than your doctor recommended.
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