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Tradol Side Effects

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Common Tradol Side Effects


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

Post Herpetic Neuralgia (2)
Somnolence (2)
Myalgia (2)
Headache (2)
Dizziness (2)
Hallucination (2)
Confusional State (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.

Tradol Side Effects Reported to FDA


Tradol Side Effect Report#5643334-5
Confusional State, Hallucination, Post Herpetic Neuralgia
This is a report of a 64-year-old female patient (weight: NA) from Mexico, suffering from the following health symptoms/conditions: neuropathy peripheral, who was treated with Tradol Retard (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Confusional State, Hallucination, Post Herpetic Neuralgia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tradol Retard treatment in female patients, resulting in Confusional State side effect. The patient was hospitalized.
Tradol Side Effect Report#5627930-7
Confusional State, Hallucination, Post Herpetic Neuralgia
This report suggests a potential Tradol Retard Confusional State side effect(s) that can have serious consequences. A 64-year-old female patient (weight: NA) from Mexico was diagnosed with the following symptoms/conditions: neuropathy peripheral and used Tradol Retard (dosage: NA) starting NS. After starting Tradol Retard the patient began experiencing various side effects, including: Confusional State, Hallucination, Post Herpetic NeuralgiaAdditional drugs used concurrently: NA.The patient was hospitalized. Although Tradol Retard demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Confusional State, may still occur.
Tradol Side Effect Report#5466144-0
Dizziness, Headache, Myalgia, Somnolence
This Dizziness problem was reported by a pharmacist from Ireland. A 76-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: pain. On
Jun 13, 2007 this consumer started treatment with Tradol (ngx) (tramadol) Capsule, 50mg (dosage: 50mg, Bid; Oral). The following drugs were being taken at the same time:
  • Diamicron (gliclazide)
  • Furosemide
  • Domperidone (domperidone)
  • Glucophage
  • Perindopril Erbumine
  • Amlodipine Besylate
  • Serc
  • Nu-seals Aspirin (acetylsalicylic Acid)
When using Tradol (ngx) (tramadol) Capsule, 50mg, the patient experienced the following unwanted symptoms/side effects: Dizziness, Headache, Myalgia, SomnolenceThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dizziness, may become evident only after a product is in use by the general population.
Tradol Side Effect Report#5397731-6
Dizziness, Headache, Myalgia, Somnolence
This Dizziness side effect was reported by a pharmacist from Ireland. A 76-year-old male patient (weight:NA) experienced the following symptoms/conditions: pain.The patient was prescribed Tradol (ngx)(tramadol) Capsule, 50mg (drug dosage: 50 Mg, Bid, Oral), which was initiated on
Jun 13, 2007. Concurrently used drugs:
  • Diamicron (gliclazide)
  • Furosemide
  • Domperidone (domperidone)
  • Glucophage
  • Perindopril Erbumine
  • Amlodipine Besylate
  • Serc
  • Nu-seals Aspirin (acetylsalicylic Acid)
.After starting to take Tradol (ngx)(tramadol) Capsule, 50mg the consumer reported adverse symptoms, such as: Dizziness, Headache, Myalgia, SomnolenceThese side effects may potentially be related to Tradol (ngx)(tramadol) Capsule, 50mg. The patient was hospitalized.


The appearance of Tradol 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 Tradol Side Effects for Women?

Women Side EffectsReports
Confusional State 2
Hallucination 2
Post Herpetic Neuralgia 2

What are common Tradol Side Effects for Men?

Men Side EffectsReports
Dizziness 2
Headache 2
Myalgia 2
Somnolence 2

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.

    Tradol 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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