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Feosol Side Effects

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Common Feosol Side Effects


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

Urticaria (1)
Haemoglobin Decreased (1)
Glossodynia (1)
Adrenal Insufficiency (1)
Unevaluable Event (1)
Throat Tightness (1)
Pain In Jaw (1)
Renal Failure Acute (1)
Staphylococcus Test Positive (1)
Postoperative Ileus (1)
Rectal Haemorrhage (1)
Emotional Distress (1)
Gastrointestinal Stoma Complication (1)
Gingival Pain (1)
Constipation (1)
Candidiasis (1)
Renal Failure (1)
Anaphylactic Reaction (1)
Burning Mouth Syndrome (1)
Weight Decreased (1)

➢ More



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.

Feosol Side Effects Reported to FDA



Feosol Side Effect Report#9781089
Urticaria, Anaphylactic Reaction, Throat Tightness
This is a report of a 35-year-old female patient (weight: NA) from US, suffering from the following health symptoms/conditions: anaemia postoperative,urticaria, who was treated with Feosol Ferrous Sulfate Iron (dosage: 65 Mg, 1 In 1 D, start time:
Dec 13, 2013), combined with:
  • Benadryl
  • Gentamicin
  • Ativan
  • Synthroid
and developed a serious reaction and side effect(s): Urticaria, Anaphylactic Reaction, Throat Tightness after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Feosol Ferrous Sulfate Iron treatment in female patients, resulting in Urticaria side effect.
Feosol Side Effect Report#9486919
Abdominal Pain Upper, Constipation
This report suggests a potential Feosol Abdominal Pain Upper side effect(s) that can have serious consequences. A 79-year-old female patient (weight: NA) from US was diagnosed with the following symptoms/conditions: blood count abnormal and used Feosol (dosage: NA) starting 2006. After starting Feosol the patient began experiencing various side effects, including: Abdominal Pain Upper, ConstipationAdditional drugs used concurrently: NA.The patient was hospitalized. Although Feosol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abdominal Pain Upper, may still occur.
Feosol Side Effect Report#8437692-6
Candidiasis, Pain In Jaw, Glossodynia, Gingival Pain, Burning Mouth Syndrome, Oral Pain
This Candidiasis problem was reported by a physician from United States. A 73-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 21, 2012 this consumer started treatment with Feosol (dosage: NA). The following drugs were being taken at the same time:
  • B12 /00056201/
  • Prilosec
  • Omeprazole
  • Crestor
  • Zoloft
  • Calcium + Vitamin D /01483701/
  • Plaquenil
  • Sertraline Hydrochloride
When using Feosol, the patient experienced the following unwanted symptoms/side effects: Candidiasis, Pain In Jaw, Glossodynia, Gingival Pain, Burning Mouth Syndrome, Oral PainAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Candidiasis, may become evident only after a product is in use by the general population.
Feosol Side Effect Report#7938908-2
Intestinal Strangulation, Haemoglobin Decreased
This Intestinal Strangulation side effect was reported by a health professional from Canada. A female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Feosol (drug dosage: NA), which was initiated on
Sep 22, 2011. Concurrently used drugs:
  • Remicade
  • Folic Acid
  • Methotrexate
  • Bisoprolol Fumarate
  • Vitamin D (1000 Units)
  • Dabigatran
  • Vitamin B-12
  • Metformin
.After starting to take Feosol the consumer reported adverse symptoms, such as: Intestinal Strangulation, Haemoglobin DecreasedThese side effects may potentially be related to Feosol. The patient was hospitalized.
Feosol Side Effect Report#7396365-1
Renal Failure Acute, Pain, Renal Failure, Unevaluable Event, Injury, Emotional Distress
This is a report of a male patient (weight: NA) from United States, suffering from the following health symptoms/conditions: NA, who was treated with Feosol (dosage: Unk, start time:
Feb 23, 2006), combined with:
  • Heparin (6000 Units, X2)
  • Propofol (40 Mg, Unk)
  • Thiopental Sodium (40 Mg, Unk)
  • Acetylsalicylic Acid Srt (Unk)
  • Duoneb (Unk)
  • Apresoline (Unk)
  • Versed (9 Mg, Unk)
  • Papaverine (Unk)
and developed a serious reaction and side effect(s): Renal Failure Acute, Pain, Renal Failure, Unevaluable Event, Injury, Emotional Distress after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Feosol treatment in male patients, resulting in Renal Failure Acute side effect. The patient was hospitalized.
Feosol Side Effect Report#7322915-7
Weight Decreased, Postoperative Ileus, Hyponatraemia, Gastrointestinal Stoma Complication, Staphylococcus Test Positive, Rectal Haemorrhage, Adrenal Insufficiency
This report suggests a potential Feosol Weight Decreased side effect(s) that can have serious consequences. A male patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: NA and used Feosol (dosage: NA) starting NS. After starting Feosol the patient began experiencing various side effects, including: Weight Decreased, Postoperative Ileus, Hyponatraemia, Gastrointestinal Stoma Complication, Staphylococcus Test Positive, Rectal Haemorrhage, Adrenal InsufficiencyAdditional drugs used concurrently:
  • Acetaminophen
  • Hydrocodone Bitartrate
  • Prednisone
  • Probiotics
  • Infliximab, Recombinant
  • Morphine
  • Infliximab, Recombinant
The patient was hospitalized. Although Feosol demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Weight Decreased, may still occur.


The appearance of Feosol 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.


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.

    Feosol 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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    Side Effects reported to FDA: 6

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    Reported hospitalizations: 4

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