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Tilcotil Side Effects

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Common Tilcotil Side Effects


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

Cytolytic Hepatitis (2)
Anaemia (2)
Alanine Aminotransferase Increased (2)
Haemoglobin Decreased (2)
Antibody Test Positive (2)
Leukopenia (2)
Lupus-like Syndrome (2)
Lymphopenia (2)
Gait Disturbance (1)
Headache (1)
Dizziness (1)
Cognitive Disorder (1)
Leukoencephalopathy (1)
Bone Pain (1)
Muscular Weakness (1)
Paraesthesia (1)
Muscle Spasms (1)
Muscle Rigidity (1)
Motor Dysfunction (1)
Memory Impairment (1)

➢ More



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.

Tilcotil Side Effects Reported to FDA


Tilcotil Side Effect Report#7389366-0
Memory Impairment, Cognitive Disorder, Dizziness, Paraesthesia, Amnesia, Headache, Leukoencephalopathy, Somnolence, Motor Dysfunction
This is a report of a 70-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: pain, who was treated with Tilcotil (dosage: 20mg Per Day, start time:
Jun 01, 2010), combined with:
  • Tareg (80mg Per Day)
  • Acetaminophen W/ Codeine (1g Per Day)
  • Cymbalta
  • Lexomil (12mg Per Day)
  • Mestinon (2unit Per Day)
  • Ropinirole Hydrochloride (3mg Per Day)
and developed a serious reaction and side effect(s): Memory Impairment, Cognitive Disorder, Dizziness, Paraesthesia, Amnesia, Headache, Leukoencephalopathy, Somnolence, Motor Dysfunction after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tilcotil treatment in female patients, resulting in Memory Impairment side effect. The patient was hospitalized.
Tilcotil Side Effect Report#7270777-9
Bone Pain, Muscular Weakness, Muscle Rigidity, Gait Disturbance, Muscle Spasms
This report suggests a potential Tilcotil Bone Pain side effect(s) that can have serious consequences. A 77-year-old male patient (weight: NA) from Portugal was diagnosed with the following symptoms/conditions: NA and used Tilcotil (dosage: Unk) starting
Dec 29, 2010. After starting Tilcotil the patient began experiencing various side effects, including: Bone Pain, Muscular Weakness, Muscle Rigidity, Gait Disturbance, Muscle SpasmsAdditional drugs used concurrently:
  • Lyrica (75 Mg, 2x/day)
  • Xanax (Unk)
  • Nolotil /spa/ (Unk)
  • Acetaminophen (1000 Mg, Unk)
Although Tilcotil demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Bone Pain, may still occur.
Tilcotil Side Effect Report#5609001-9
Alanine Aminotransferase Increased, Anaemia, Antibody Test Positive, Cytolytic Hepatitis, Haemoglobin Decreased, Leukopenia, Lupus-like Syndrome, Lymphopenia
This Alanine Aminotransferase Increased problem was reported by a consumer or non-health professional from France. A 58-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: arthralgia. On
Mar 05, 2007 this consumer started treatment with Tilcotil (dosage: 20 Mg, Qd). The following drugs were being taken at the same time:
  • Voltaren (75 Mg, Qd)
When using Tilcotil, the patient experienced the following unwanted symptoms/side effects: Alanine Aminotransferase Increased, Anaemia, Antibody Test Positive, Cytolytic Hepatitis, Haemoglobin Decreased, Leukopenia, Lupus-like Syndrome, LymphopeniaThe 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 Alanine Aminotransferase Increased, may become evident only after a product is in use by the general population.
Tilcotil Side Effect Report#5594315-1
Alanine Aminotransferase Increased, Anaemia, Antibody Test Positive, Cytolytic Hepatitis, Haemoglobin Decreased, Leukopenia, Lupus-like Syndrome, Lymphopenia
This Alanine Aminotransferase Increased side effect was reported by a consumer or non-health professional from France. A 58-year-old male patient (weight:NA) experienced the following symptoms/conditions: arthralgia.The patient was prescribed Tilcotil (drug dosage: 20 Mg, Qd), which was initiated on
Mar 05, 2007. Concurrently used drugs:
  • Voltaren (75 Mg, Qd)
.After starting to take Tilcotil the consumer reported adverse symptoms, such as: Alanine Aminotransferase Increased, Anaemia, Antibody Test Positive, Cytolytic Hepatitis, Haemoglobin Decreased, Leukopenia, Lupus-like Syndrome, LymphopeniaThese side effects may potentially be related to Tilcotil. The patient was hospitalized.



The appearance of Tilcotil 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.

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.

    Tilcotil 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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    Tilcotil Safety Alerts, Active Ingredients, Usage Information

    More About Tilcotil

    Side Effects reported to FDA: 4

    Tilcotil safety alerts: No

    Reported hospitalizations: 3

    Latest Tilcotil clinical trials