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Siofor Side Effects

Common Siofor Side Effects


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

Dehydration (1)
Dermatitis Allergic (1)
Cholecystectomy (1)
Blood Glucose Increased (1)
Ureteric Obstruction (1)
Diabetes Mellitus (1)
Eczema (1)
Syncope (1)
Ureteral Disorder (1)
Paranoia (1)
Lichenoid Keratosis (1)
Hallucination (1)
Atrioventricular Block Complete (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.

Siofor Side Effects Reported to FDA

The following Siofor 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 Siofor 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.
Diabetes Mellitus, Dehydration
This is a report of a 50-year-old female patient (weight: NA) from COUNTRY NOT SPECIFIED, suffering from the following symptoms/conditions: NA, who was treated with Siofor (dosage: 3000 Mg, start time: Jul 03, 2013), combined with:
  • Metoprolol Tartrate (200 Mg)
  • Amlodipin (10 Mg)
  • Ebrantil (120 Mg)
  • Tritazide (5/25 Mg)
  • Telmisartan (80 Mg)
  • Anopyrin (200 Mg)
  • Anopyrin (100 Mg)
  • Heparine (5000)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Diabetes Mellitus
  • Dehydration
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Siofor treatment in female patients, resulting in diabetes mellitus side effect. The patient was hospitalized.

Syncope, Atrioventricular Block Complete
This report suggests a potential Siofor Syncope, Atrioventricular Block Complete side effect(s) that can have serious consequences. A 68-year-old female patient (weight: NA) from ROMANIA was diagnosed with the following symptoms/conditions: diabetes mellitus and used Siofor (dosage: NA) starting Aug 01, 2007. Soon after starting Siofor the patient began experiencing various side effects, including:
  • Syncope
  • Atrioventricular Block Complete
Drugs used concurrently:
  • Neupro
  • Neupro
  • Neupro
  • Amaryl
The patient was hospitalized. Although Siofor demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as syncope, may still occur.

Cholecystectomy
This Cholecystectomy problem was reported by a physician from RUSSIAN FEDERATION. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: diabetes mellitus,hypertension,dyslipidaemia. On Sep 01, 2007 this consumer started treatment with Siofor (dosage: NA). The following drugs were being taken at the same time:
  • Enalapril Maleate
  • Fenofibrate
  • Tricor
When commencing Siofor, the patient experienced the following unwanted symptoms/side effects:
  • Cholecystectomy
The 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 cholecystectomy, may become evident only after a product is in use by the general population.

Eczema, Lichenoid Keratosis
This is a report of a 57-year-old female patient (weight: NA) from SLOVAKIA (Slovak Republic). The patient developed the following symptoms/conditions: NA and was treated with Siofor (dosage: 500 Mg, Bid) starting NS. Concurrently used drugs:
  • Caltrate Plus /01438001/
  • Humalog (20018 Unk, Unk)
  • Levothyroxine Sodium (125 Mg, Qd)
  • Prolia
  • Bisoprolol Fumarate And Hydrochlorothiazide
Soon after that, the consumer experienced the following side effects:
  • Eczema
  • Lichenoid Keratosis
The patient was hospitalized. This opens a possibility that Siofor treatment could cause the above reactions, including eczema, and some female subjects may be more susceptible.


Paranoia, Hallucination
A 59-year-old male patient (weight: NA) from GERMANY with the following symptoms/conditions: diabetes mellitus,schizophrenia,parkinsonism started Siofor treatment (dosage: 1700 Mg, Unk) on Nov 01, 2006. Soon after starting Siofor treatment, the subject experienced various side effects, including:
  • Paranoia
  • Hallucination
Concurrently used drugs:
  • Olanzapine Long-acting Im (210 Mg, Unk)
  • Biperiden Hydrochloride Tab (10 Mg, Unk)
The patient was hospitalized. This finding indicates that some male patients could be more vulnerable to Siofor.

Blood Glucose Increased, Ureteric Obstruction, Ureteral Disorder
A 68-year-old male patient from GERMANY (weight: NA) experienced symptoms, such as: NA and was treated with Siofor(dosage: 1000 D/f, Unk). The treatment was initiated on NS. After that a consumer reported the following side effect(s):
  • Blood Glucose Increased
  • Ureteric Obstruction
  • Ureteral Disorder
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Siofor efficacy:
  • Simvastatin (20 Mg, Unk)
  • Byetta
  • Delix (2.5 Mg, Unk)
  • Nexium-mups /01479302/ (40 Mg, Unk)
  • Betapressin
  • Valoron N
The patient was hospitalized.

Dermatitis Allergic
In this report, Siofor was administered for the following condition: NA.A 50-year-old female consumer from UKRAINE (weight: NA) started Siofor treatment (dosage: NA) on NS.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Dermatitis Allergic
A possible interaction with other drugs could have contributed to this reaction:
  • Amaryl
  • Byetta (0.25 Mg, 2/d)
Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Siofor treatment could be related to the listed above side effect(s).



Top 10 Siofor Side Effects for Men

Men Side EffectsReports
Blood Glucose Increased 1
Hallucination 1
Paranoia 1
Ureteral Disorder 1
Ureteric Obstruction 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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    Siofor Safety Alerts, Active Ingredients, Usage Information

    More About Siofor

    Side Effects reported to FDA: 7

    Siofor safety alerts: No

    Reported hospitalizations: 6

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