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Ritalina Side Effects and Adverse Effects reported to US Food and Drug Administration (FDA)

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Henoch-schonlein Purpura (7341840-9)
on Feb 25, 2011 Male from GERMANY , weighting 69.23 lb, was diagnosed with
  • attention deficit/hyperactivity disorder
and was treated with Ritalina La. Directly after, patient experienced the unwanted or unexpected Ritalina side effects: henoch-schonlein purpura. Ritalina La dosage: 20 Mg, Unk.
Associated medications used:
  • Strattera (35 Mg, Daily (1/d))


Body Height Increased, Increased Appetite, Weight Increased (4563858-1)
Patient was taking Ritalina. Patient felt the following Ritalina side effects: body height increased, increased appetite, weight increased on Jan 20, 2005 from Additional patient health information: Male , 15 years of age, weighting 88.18 lb, was diagnosed with
  • dyslexia
and. Ritalina dosage: 3 Df/day.

Syncope (4563857-X)
Adverse event was reported on Jan 20, 2005 by a Female taking Ritalina (Dosage: N/A) . Location: , 46 years of age, After Ritalina was administered, patient encountered several Ritalina side effects: syncope.

Body Height Increased, Increased Appetite, Weight Increased (4561221-0)
on Jan 20, 2005 Male from , 15 years of age, weighting 88.18 lb, was diagnosed with
  • dyslexia
and was treated with Ritalina. Directly after, patient experienced the unwanted or unexpected Ritalina side effects: body height increased, increased appetite, weight increased. Ritalina dosage: 3 Df/day.


Syncope (4559085-4)
on Jan 20, 2005 Female from , 46 years of age, was treated with Ritalina. Patient felt the following Ritalina side effects: syncope. Ritalina dosage: N/A.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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