Prothiaden Side Effects


Common Prothiaden Side Effects

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

Hypoglycaemia Neonatal (1)
Hypocalcaemia (1)
Completed Suicide (1)
Abortion Induced (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.

Prothiaden Side Effects Reported to FDA

Prothiaden Side Effect Report#7715509-2
Hypocalcaemia, Hypoglycaemia Neonatal
This is a report of a female patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Prothiaden (dosage: 25 Mg (25 Mg, 1 In 1 D), Transplacental, start time: NS), combined with:
  • Nebivolol Hcl (Transplacental)
and developed a serious reaction and side effect(s): Hypocalcaemia, Hypoglycaemia Neonatal after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Prothiaden treatment in female patients, resulting in Hypocalcaemia side effect. The patient was hospitalized.
Prothiaden Side Effect Report#4967307-0
Abortion Induced
This report suggests a potential Prothiaden Abortion Induced side effect(s) that can have serious consequences. A 33-year-old female patient (weight: NA) from United Kingdom was diagnosed with the following symptoms/conditions: NA and used Prothiaden (dosage: NA) starting NS. After starting Prothiaden the patient began experiencing various side effects, including: Abortion InducedAdditional drugs used concurrently: NA. Although Prothiaden demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abortion Induced, may still occur.
Prothiaden Side Effect Report#4750442-X
Completed Suicide
This Completed Suicide problem was reported by a consumer or non-health professional from Australia. A 53-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Mar 11, 2005 this consumer started treatment with Prothiaden (dosage: NA). The following drugs were being taken at the same time:
  • Zometa
When using Prothiaden, the patient experienced the following unwanted symptoms/side effects: Completed SuicideAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Completed Suicide, may become evident only after a product is in use by the general population.

The appearance of Prothiaden 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 Prothiaden Side Effects for Women?

Women Side EffectsReports
Abortion Induced 1
Hypocalcaemia 1
Hypoglycaemia Neonatal 1

What are common Prothiaden Side Effects for Men?

Men Side EffectsReports
Completed Suicide 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.

    Prothiaden 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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