Common Prometax Side Effects

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

Flight Of Ideas (1)
Hypernatraemia (1)
Fatigue (1)
Disorientation (1)
Vomiting (1)
Bradycardia (1)
Inappropriate Affect (1)
Insomnia (1)
Oedema Peripheral (1)
Speech Disorder (1)
Muscular Weakness (1)
Mania (1)
Loss Of Consciousness (1)
Aggression (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.

Prometax Side Effects Reported to FDA

Prometax Side Effect Report#9358433
Oedema Peripheral
This is a report of a 71-year-old male patient (weight: NA) from Country Not Specified, suffering from the following health symptoms/conditions: dementia alzheimer^s type, who was treated with Prometax (dosage: 1.5 Mg, Unk, start time:
Sep 12, 2012), combined with: NA. and developed a serious reaction and side effect(s): Oedema Peripheral after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Prometax treatment in male patients, resulting in Oedema Peripheral side effect.
Prometax Side Effect Report#8887133
Hypernatraemia, Disorientation, Muscular Weakness, Vomiting, Fatigue
This report suggests a potential Prometax Hypernatraemia side effect(s) that can have serious consequences. A 80-year-old male patient (weight: NA) from PT was diagnosed with the following symptoms/conditions: dementia alzheimer^s type and used Prometax (dosage: 4.6 Mg/24 Hour) starting NS. After starting Prometax the patient began experiencing various side effects, including: Hypernatraemia, Disorientation, Muscular Weakness, Vomiting, FatigueAdditional drugs used concurrently:
  • Domperidone
  • Memantine
The patient was hospitalized. Although Prometax demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hypernatraemia, may still occur.
Prometax Side Effect Report#5405628-8
Aggression, Flight Of Ideas, Inappropriate Affect, Insomnia, Mania, Speech Disorder
This Aggression problem was reported by a health professional from Portugal. A 56-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: dementia. On
Jan 01, 2007 this consumer started treatment with Prometax (dosage: 3 Mg, Unk). The following drugs were being taken at the same time:
  • Alprazolam (6 Mg, Qd)
  • Sinemet
  • Venlafaxine Hcl (150 Mg, Qd)
  • Selegiline Hydrochloride
When using Prometax, the patient experienced the following unwanted symptoms/side effects: Aggression, Flight Of Ideas, Inappropriate Affect, Insomnia, Mania, Speech DisorderThe 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 Aggression, may become evident only after a product is in use by the general population.
Prometax Side Effect Report#5272325-1
Bradycardia, Loss Of Consciousness
This Bradycardia side effect was reported by a consumer or non-health professional from Portugal. A 82-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Prometax (drug dosage: 6 Mg/d), which was initiated on
Jan 01, 2004. Concurrently used drugs:
  • Donepezil Hcl
  • Lorazepam
  • Tocopheryl Acetate
  • Sertraline
.After starting to take Prometax the consumer reported adverse symptoms, such as: Bradycardia, Loss Of ConsciousnessThese side effects may potentially be related to Prometax. The patient was hospitalized and became disabled.

The appearance of Prometax 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 Prometax Side Effects for Women?

Women Side Effects Reports
Aggression 1
Bradycardia 1
Flight Of Ideas 1
Inappropriate Affect 1
Insomnia 1
Loss Of Consciousness 1
Mania 1
Speech Disorder 1

What are common Prometax Side Effects for Men?

Men Side Effects Reports
Disorientation 1
Fatigue 1
Hypernatraemia 1
Muscular Weakness 1
Oedema Peripheral 1
Vomiting 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.

    Prometax 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 Prometax

    Side Effects reported to FDA: 4

    Prometax safety alerts: No

    Reported hospitalizations: 3

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