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Stemetil Side Effects

Common Stemetil Side Effects


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

Gastrointestinal Ulcer (1)
Haematemesis (1)
Fall (1)
Emotional Disorder (1)
Urinary Tract Infection (1)
Dizziness (1)
Hospitalisation (1)
Loss Of Consciousness (1)
Partial Seizures (1)
Upper Gastrointestinal Haemorrhage (1)
Oesophagitis (1)
Neutropenia (1)
Myoclonus (1)
Completed Suicide (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.

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.

Stemetil Side Effects Reported to FDA

The following Stemetil 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.


The appearance of Stemetil 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.
Hospitalisation
This is a report of a male patient (weight: NA) from CANADA, suffering from the following symptoms/conditions: crohn's disease, who was treated with Stemetil (dosage: NA, start time: Jul 07, 2011), combined with:
  • Sulfasalazine
  • Maxeran
  • Kaletra (200/50mg)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Hospitalisation
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Stemetil treatment in male patients, resulting in hospitalisation side effect. The patient was hospitalized.

Neutropenia
This report suggests a potential Stemetil Neutropenia side effect(s) that can have serious consequences. A male patient (weight: NA) from CANADA was diagnosed with the following symptoms/conditions: NA and used Stemetil (dosage: NA) starting Mar 04, 2011. Soon after starting Stemetil the patient began experiencing various side effects, including:
  • Neutropenia
Drugs used concurrently:
  • Zofran
  • Imodium
  • Pariet
  • Pepcid
  • Emend
  • Fragmin
  • Oxaliplatin
  • Pantoloc
The patient was hospitalized. Although Stemetil demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as neutropenia, may still occur.

Completed Suicide, Emotional Disorder
This Completed Suicide, Emotional Disorder problem was reported by a health professional from DENMARK. A 66-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Stemetil (prochloroperazine) (dosage: NA). The following drugs were being taken at the same time:
  • Celexa (10 Mg (10 Mg, 1 In 1 D), Oral)
When commencing Stemetil (prochloroperazine), the patient experienced the following unwanted symptoms/side effects:
  • Completed Suicide
  • Emotional Disorder
Although 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.

Oesophagitis, Urinary Tract Infection, Haematemesis, Gastrointestinal Ulcer, Fall, Dizziness, Loss Of Consciousness, Upper Gastrointestinal Haemorrhage
This is a report of a 66-year-old female patient (weight: NA) from DENMARK. The patient developed the following symptoms/conditions: NA and was treated with Stemetil (dosage: NA) starting Oct 02, 2009. Concurrently used drugs:
  • Zopiclone
  • Citalopram Hydrobromide (20 Mg; Qd; Po)
  • Clozaril (400 Mg; Qd; Po)
  • Ismo
  • Simvastatin
Soon after that, the consumer experienced the following side effects:
  • Oesophagitis
  • Urinary Tract Infection
  • Haematemesis
  • Gastrointestinal Ulcer
  • Fall
  • Dizziness
  • Loss Of Consciousness
  • Upper Gastrointestinal Haemorrhage
The patient was hospitalized. This opens a possibility that Stemetil treatment could cause the above reactions, including oesophagitis, and some female subjects may be more susceptible.


Myoclonus, Partial Seizures
A 50-year-old female patient (weight: NA) from SOUTH AFRICA with the following symptoms/conditions: helicobacter infection started Stemetil treatment (dosage: NA) on Sep 06, 2009. Soon after starting Stemetil treatment, the subject experienced various side effects, including:
  • Myoclonus
  • Partial Seizures
Concurrently used drugs:
  • Nexium (Unk)
  • Synap Forte (Unk)
  • Brazepam
  • Stilnox (Unk)
  • Stilnox Mr
The patient was hospitalized. This finding indicates that some female patients could be more vulnerable to Stemetil.



Top 10 Stemetil Side Effects for Men

Men Side EffectsReports
Completed Suicide 1
Emotional Disorder 1
Hospitalisation 1
Neutropenia 1

Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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

    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.


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