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Sormodren Side Effects

Common Sormodren Side Effects


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

Fall (1)
Overdose (1)
Disorientation (1)
Diplopia (1)
Confusional State (1)
Ankle Fracture (1)


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.

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.

Sormodren Side Effects Reported to FDA

The following Sormodren 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.


The appearance of Sormodren 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.
Diplopia
This is a report of a male patient (weight: NA) from GERMANY, suffering from the following symptoms/conditions: salivary hypersecretion,parkinson's disease,myalgia, who was treated with Sormodren (dosage: NA, start time: NS), combined with:
  • Madopar
  • Meloxicam
  • Requip (4mg Three Times Per Day)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Diplopia
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Sormodren treatment in male patients, resulting in diplopia side effect.

Ankle Fracture, Disorientation, Overdose, Confusional State, Fall
This report suggests a potential Sormodren Ankle Fracture, Disorientation, Overdose, Confusional State, Fall side effect(s) that can have serious consequences. A female patient (weight: NA) from UNITED STATES was diagnosed with the following symptoms/conditions: NA and used Sormodren (dosage: 1-0-1) starting NS. Soon after starting Sormodren the patient began experiencing various side effects, including:
  • Ankle Fracture
  • Disorientation
  • Overdose
  • Confusional State
  • Fall
Drugs used concurrently:
  • Movicol /01053601/ (1-1-1)
  • Acc Long (1-0-0)
  • Exalgo (8 Mg + 8 Mg + 8 Mg, Bid)
  • Wobenzym /00598501/ (1-1-1)
  • Busp (In 1 As Necessary)
  • Exalgo (16 Mg + 8 Mg , Bid)
  • Rabeprazole Sodium (1 Unk, Unk)
  • Lexotanil (6 Mg 1-0-1)
The patient was hospitalized. Although Sormodren demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as ankle fracture, may still occur.



Top 10 Sormodren Side Effects for Women

Women Side EffectsReports
Ankle Fracture 1
Confusional State 1
Disorientation 1
Fall 1
Overdose 1

Top 10 Sormodren Side Effects for Men

Men Side EffectsReports
Diplopia 1

Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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

    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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    Sormodren Safety Alerts, Active Ingredients, Usage Information

    More About Sormodren

    Side Effects reported to FDA: 2

    Sormodren safety alerts: No

    Reported hospitalizations: 1

    Latest Sormodren clinical trials

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