Common Neurovitan Side Effects

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

Immunodeficiency (1)
Metastatic Pain (1)
Hyponatraemia (1)
Femoral Neck Fracture (1)
Vasculitis (1)
Disuse Syndrome (1)
Overdose (1)
Pain In Extremity (1)
Quality Of Life Decreased (1)
Tremor (1)
Postrenal Failure (1)
Papillophlebitis (1)
Papilloedema (1)
Carcinoembryonic Antigen Increased (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.

Neurovitan Side Effects Reported to FDA

Neurovitan Side Effect Report#7996308-3
Postrenal Failure, Carcinoembryonic Antigen Increased, Tremor, Metastatic Pain, Overdose
This is a report of a female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Neurovitan /00280501/ (dosage: 1 Tablet, Tid, start time:
Nov 20, 2011), combined with:
  • Methadone Hcl (20 Mg, Bid)
  • Diart (30 Mg, Qd)
  • Methadone Hcl (15 Mg, Bid)
  • Sodium Chloride (100 Ml, Once/four Weeks)
  • Azunol /00317302/ (Adequate Dose)
  • Methadone Hcl (10 Mg, Bid)
  • Methadone Hcl (25 Mg, Bid)
  • Hirudoid /00723701/ (Adequate Dose For External Use)
and developed a serious reaction and side effect(s): Postrenal Failure, Carcinoembryonic Antigen Increased, Tremor, Metastatic Pain, Overdose after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Neurovitan /00280501/ treatment in female patients, resulting in Postrenal Failure side effect. The patient was hospitalized.
Neurovitan Side Effect Report#7604398-2
Femoral Neck Fracture, Quality Of Life Decreased, Pain In Extremity, Papillophlebitis, Vasculitis, Immunodeficiency, Papilloedema, Disuse Syndrome
This report suggests a potential Neurovitan /00176001/ (cyanocobalamin, Pyridoxine Hydrochloride,thiami Femoral Neck Fracture side effect(s) that can have serious consequences. A 53-year-old male patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Neurovitan /00176001/ (cyanocobalamin, Pyridoxine Hydrochloride,thiami (dosage: NA) starting
May 06, 2005. After starting Neurovitan /00176001/ (cyanocobalamin, Pyridoxine Hydrochloride,thiami the patient began experiencing various side effects, including: Femoral Neck Fracture, Quality Of Life Decreased, Pain In Extremity, Papillophlebitis, Vasculitis, Immunodeficiency, Papilloedema, Disuse SyndromeAdditional drugs used concurrently:
  • Livact /00847901/ (valine, Leucine, Isoleucine)
  • Anplag (sarpogrelate Hydrochloride)
  • Allopurinol
  • Takepron (lansoprazole)
  • Tulobuterol (tulobuterol)
  • Lactulose
  • Methycobal /00324901/ (mecobalamin)
  • Ketoprofen
The patient was hospitalized and became disabled. Although Neurovitan /00176001/ (cyanocobalamin, Pyridoxine Hydrochloride,thiami demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Femoral Neck Fracture, may still occur.
Neurovitan Side Effect Report#7501909-2
This Hyponatraemia problem was reported by a physician from Japan. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: prophylaxis,ovarian cancer. On
Apr 07, 2011 this consumer started treatment with Neurovitan (dosage: NA). The following drugs were being taken at the same time:
  • Doxil
  • Doxil
  • Carboplatin
  • Dermovate
  • Kytril
  • Mucosta
  • Decadron
  • Azunol
When using Neurovitan, the patient experienced the following unwanted symptoms/side effects: HyponatraemiaThe 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 Hyponatraemia, may become evident only after a product is in use by the general population.

The appearance of Neurovitan 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 Neurovitan Side Effects for Women?

Women Side Effects Reports
Carcinoembryonic Antigen Increased 1
Hyponatraemia 1
Metastatic Pain 1
Overdose 1
Postrenal Failure 1
Tremor 1

What are common Neurovitan Side Effects for Men?

Men Side Effects Reports
Disuse Syndrome 1
Femoral Neck Fracture 1
Immunodeficiency 1
Pain In Extremity 1
Papilloedema 1
Papillophlebitis 1
Quality Of Life Decreased 1
Vasculitis 1

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.

    Neurovitan 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 Neurovitan

    Side Effects reported to FDA: 3

    Neurovitan safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 1

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