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

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Pulmonary Embolism, Jugular Vein Thrombosis (8246645-2)
on Feb 27, 2012 Male from FRANCE , 59 years of age, was treated with Augmentine (augmentine). Directly after, patient experienced the unwanted or unexpected Augmentine side effects: pulmonary embolism, jugular vein thrombosis. Augmentine (augmentine) dosage: N/A.
Associated medications used:
  • Tachosil (1 Sponge 9.5 Cm X 4.8 Cm)
  • Zolpidem Tartrate
  • Haldol (haloperidol Decanoate) (2 Milligram/milliliters)
  • Acetaminophen
  • Amlor (amlodipne Besilate)

Deep Vein Thrombosis (7703312-9)
Patient was taking Augmentine /00852501/. Patient felt the following Augmentine side effects: deep vein thrombosis on Aug 09, 2011 from SPAIN Additional patient health information: Female , weighting 143.3 lb, was diagnosed with
  • cellulitis
  • pain
and. Augmentine /00852501/ dosage: 3 Df, Qd.
Multiple prescriptions taken:
  • Acetaminophen (3 Df, Qd)
  • Nolotil (3 Df, Qd)
  • Diazepan (1 Df, Qd)
  • Enoxaparin Sodium (1 Df, Bid)
  • Norvasc (1 Df, Qd)
  • Forteo (20 Ug, Qd)
  • Omeprazole (1 Df, Qd)

Oedema, Pruritus (5679010-2)
Adverse event was reported on Mar 18, 2008 by a Male taking Augmentine (oral) (Dosage: N/A) was diagnosed with
  • oral infection
and. Location: SPAIN , 75 years of age, After Augmentine was administered, patient encountered several Augmentine side effects: oedema, pruritus.

Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Blood Phosphorus Increased, Cholestasis (5663143-0)
on Mar 07, 2008 Male from SWITZERLAND , 34 years of age, was diagnosed with
  • prophylaxis
and was treated with Augmentine (oral). Directly after, patient experienced the unwanted or unexpected Augmentine side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood phosphorus increased, cholestasis. Augmentine (oral) dosage: N/A. Patient was hospitalized.

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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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