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Drug Interaction (1)
Dry Mouth (1)
Nausea (1)
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Ultran Side Effects and Adverse Effects reported to US Food and Drug Administration (FDA)

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Diarrhoea (7312134-2)
on Feb 15, 2011 Male from UNITED STATES , 36 years of age, was treated with Ultran. Directly after, patient experienced the unwanted or unexpected Ultran side effects: diarrhoea. Ultran dosage: 50 Mg, Unk.
Associated medications used:
  • Arthrotec (15/200 Bid)
  • Arthrotec
  • Flexeril (10 Mg, Unk)

Product Substitution Issue (7228048-2)
Patient was taking Ultran. Patient felt the following Ultran side effects: product substitution issue on Jan 12, 2011 from UNITED STATES Additional patient health information: Female , weighting 179.0 lb, was diagnosed with
  • osteoarthritis
and. Ultran dosage: 50 Mg One To Two Every Four Hours For Osteoarthrosis.

Abdominal Pain Upper, Amnesia, Depression, Influenza Like Illness, Lethargy, Withdrawal Syndrome (6256019-1)
Adverse event was reported on Jun 30, 2009 by a Female taking Ultran Tab (Dosage: 200 Mg 1 To 2x/day Po) was diagnosed with
  • back pain
and. Location: UNITED STATES , 43 years of age, weighting 170.0 lb, After Ultran was administered, patient encountered several Ultran side effects: abdominal pain upper, amnesia, depression, influenza like illness, lethargy, withdrawal syndrome.

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It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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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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