Cernilton Side Effects


Common Cernilton Side Effects

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

Dysarthria (1)
Erysipelas (1)
Death (1)
Cerebral Infarction (1)
Visual Impairment (1)
Grip Strength Decreased (1)
Interstitial Lung Disease (1)
Pyrexia (1)
Pneumonia Aspiration (1)
Phlebitis (1)
Lymphadenitis (1)
Abasia (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.

Cernilton Side Effects Reported to FDA

Cernilton Side Effect Report#8386042-2
Interstitial Lung Disease
This is a report of a 85-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: dysuria, who was treated with Cernilton (dosage: Daily Dose 189 Mg, start time:
May 06, 2011), combined with:
  • Ampicillin (Daily Dose 4 G)
  • Avelox (400 Mg, Qd)
  • Miya Bm (Daily Dose 3 G)
  • Flivastatin Sodium (Daily Dose 50 Mg)
  • Torsemide (Daily Dose 4 Mg)
  • Ampicillin Sodium W/sulbactram Sodium (Daily Dose 6 G)
  • Avelox
and developed a serious reaction and side effect(s): Interstitial Lung Disease after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Cernilton treatment in male patients, resulting in Interstitial Lung Disease side effect. The patient was hospitalized.
Cernilton Side Effect Report#8072532-9
Visual Impairment
This report suggests a potential Cernilton Death side effect(s) that can have serious consequences. A 74-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Cernilton (dosage: 6 Df, 1x/day) starting
Nov 01, 2011. After starting Cernilton the patient began experiencing various side effects, including: Visual ImpairmentAdditional drugs used concurrently:
  • Zolpidem (1 Tablet Daily)
  • Januvia (1 Tablet Daily)
  • Vfend (300 Mg, 1x/day)
  • Mucodyne (3 Tablets Daily)
  • Clarithromycin (2 Tablets Daily)
  • Enteronon (3 G, 1x/day)
  • Lansoprazole (1 Tablet Daily)
  • Symmetrel (1 Tablet Daily)
Although Cernilton demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Death, may still occur.
Cernilton Side Effect Report#7543740-8
Abasia, Grip Strength Decreased, Pyrexia, Dysarthria, Pneumonia Aspiration, Cerebral Infarction
This Abasia problem was reported by a physician from Japan. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: benign prostatic hyperplasia,gastritis. On
Jan 08, 2002 this consumer started treatment with Cernilton (dosage: NA). The following drugs were being taken at the same time:
  • Protecadin
  • Cerocral
  • Diovan (40 Mg Daily Dose)
  • Aricept
  • Glyburide
When using Cernilton, the patient experienced the following unwanted symptoms/side effects: Abasia, Grip Strength Decreased, Pyrexia, Dysarthria, Pneumonia Aspiration, Cerebral InfarctionThe 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 Abasia, may become evident only after a product is in use by the general population.
Cernilton Side Effect Report#7405874-8
Lymphadenitis, Phlebitis, Erysipelas
This Lymphadenitis side effect was reported by a consumer or non-health professional from Germany. A male patient (weight:NA) experienced the following symptoms/conditions: prostatic disorder.The patient was prescribed Cernilton (drug dosage: NA), which was initiated on
May 18, 2009. Concurrently used drugs:
  • Bisoprolol (Reported As: Bisoprolol Tad)
  • Boniva
  • Gingium (Reported As: Gingium Intens 120)
  • Terazosin Hcl (Reported As: Terazosin Hexal)
  • Galacordin (Frequency: 2)
  • Calcigen D
  • Xipamid
  • Omeprazole (Reported As: Omep 20)
.After starting to take Cernilton the consumer reported adverse symptoms, such as: Lymphadenitis, Phlebitis, ErysipelasThese side effects may potentially be related to Cernilton.

The appearance of Cernilton 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 Cernilton Side Effects for Women?

Women Side EffectsReports

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.

    Cernilton 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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    Cernilton Safety Alerts, Active Ingredients, Usage Information

    More About Cernilton

    Side Effects reported to FDA: 4

    Cernilton safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 2

    Latest Cernilton clinical trials