Common Sarotex Side Effects

The most commonly reported Sarotex side effects (click to view or check a box to report):

Coma (2)
Death (2)

If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Sarotex Side Effects Reported to FDA

Sarotex Side Effect Report#5846651-9
This is a report of a 66-year-old patient (weight: NA) from Netherlands, suffering from the following health symptoms/conditions: depression, who was treated with Sarotex Retard (dosage: 25mg Per Day, start time:
Jan 31, 2008), combined with:
  • Zofran
  • Amitriptyline Hcl (85mg Per Day)
  • Rivotril (.5mg Twice Per Day)
  • Selokeen Zoc (100mg Per Day)
  • Transtec
  • Amlodipine (5mg Per Day)
  • Diovan (80mg Per Day)
  • Valsartan (25mg Per Day)
and developed a serious reaction and side effect(s): Coma after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Sarotex Retard treatment in patients, resulting in Coma side effect.
Sarotex Side Effect Report#5789061-5
This report suggests a potential Sarotex Retard Coma side effect(s) that can have serious consequences. A 66-year-old patient (weight: NA) from Netherlands was diagnosed with the following symptoms/conditions: depression and used Sarotex Retard (dosage: 25mg Per Day) starting NS. After starting Sarotex Retard the patient began experiencing various side effects, including: ComaAdditional drugs used concurrently:
  • Zofran
  • Amitriptyline Hcl (85mg Per Day)
  • Rivotril (.5mg Twice Per Day)
  • Selokeen Zoc (1000mg Per Day)
  • Transtec
  • Amlodipine (5mg Per Day)
  • Diovan (80mg Per Day)
  • Valsartan (25mg Per Day)
Although Sarotex Retard demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Coma, may still occur.

The appearance of Sarotex on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Sarotex Side Effects for Women?

Women Side Effects Reports

What are common Sarotex Side Effects for Men?

Men Side Effects Reports

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    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.

    Sarotex reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    More About Sarotex

    Side Effects reported to FDA: 2

    Sarotex safety alerts: No

    Reported deaths: 2

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