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Tardyferon Side Effects

Common Tardyferon Side Effects


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

Anaemia (6)
Oedema Peripheral (2)
Muscle Haemorrhage (2)
Renal Failure Acute (2)
Diarrhoea (2)
Headache (2)
Hypertension (2)
Agitation (1)
Melaena (1)
Metabolic Acidosis (1)
Bacterial Test Positive (1)
Acute Respiratory Distress Syndrome (1)
Biopsy Prostate (1)
Myelodysplastic Syndrome (1)
Vomiting (1)
Vascular Purpura (1)
Multi-organ Failure (1)
Back Pain (1)
Cholelithiasis (1)
Acute Pulmonary Oedema (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.

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.

Tardyferon Side Effects Reported to FDA

The following Tardyferon 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 Tardyferon 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.
Cerebral Haemorrhage, Head Injury, Pancytopenia, Anaemia, Thrombocytopenia, Polyneuropathy, Subdural Haematoma
This is a report of a female patient (weight: NA) from POLAND, suffering from the following symptoms/conditions: NA, who was treated with Tardyferon-fol (dosage: NA, start time: Apr 09, 2009), combined with:
  • Furosemide
  • Kalipoz
  • Gleevec (400 Mg Daily)
  • Gleevec (400 Mg,)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Cerebral Haemorrhage
  • Head Injury
  • Pancytopenia
  • Anaemia
  • Thrombocytopenia
  • Polyneuropathy
  • Subdural Haematoma
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Tardyferon-fol treatment in female patients, resulting in cerebral haemorrhage side effect. The patient was hospitalized.

Anaemia, Myelodysplastic Syndrome, Renal Impairment
This report suggests a potential Tardyferon /01675201/ Anaemia, Myelodysplastic Syndrome, Renal Impairment side effect(s) that can have serious consequences. A 75-year-old female patient (weight: NA) from GREECE was diagnosed with the following symptoms/conditions: NA and used Tardyferon /01675201/ (dosage: NA) starting NS. Soon after starting Tardyferon /01675201/ the patient began experiencing various side effects, including:
  • Anaemia
  • Myelodysplastic Syndrome
  • Renal Impairment
Drugs used concurrently:
  • Ambrisentan (5 Mg, Qd)
  • Aldactone
  • Lasix
  • Diovan
The patient was hospitalized. Although Tardyferon /01675201/ demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as anaemia, may still occur.

Rhinitis, Pyrexia, Vomiting, Acute Respiratory Distress Syndrome, Dyspnoea, Diarrhoea, Lung Disorder, Hypoxia
This Rhinitis, Pyrexia, Vomiting, Acute Respiratory Distress Syndrome, Dyspnoea, Diarrhoea, Lung Disorder, Hypoxia problem was reported by a health professional from DENMARK. A 21-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On Jul 01, 2011 this consumer started treatment with Tardyferon (ferrous Sulfate) (ferrous Sulfate) (dosage: NA). The following drugs were being taken at the same time:
  • Depakote
  • Escitalopram (Oral)
  • Trinordiol (levonorgestrel, Ethinylestradiol) - (levonogestrel, Ethiny
When commencing Tardyferon (ferrous Sulfate) (ferrous Sulfate), the patient experienced the following unwanted symptoms/side effects:
  • Rhinitis
  • Pyrexia
  • Vomiting
  • Acute Respiratory Distress Syndrome
  • Dyspnoea
  • Diarrhoea
  • Lung Disorder
  • Hypoxia
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 rhinitis, may become evident only after a product is in use by the general population.

Bacterial Test Positive, Haematuria, Back Pain
This is a report of a 69-year-old male patient (weight: NA) from SWITZERLAND. The patient developed the following symptoms/conditions: NA and was treated with Tardyferon (iron) (dosage: NA) starting Jun 21, 2011. Concurrently used drugs:
  • Venofer (300 Mg, Intravenous)
Soon after that, the consumer experienced the following side effects:
  • Bacterial Test Positive
  • Haematuria
  • Back Pain
The patient was hospitalized. This opens a possibility that Tardyferon (iron) treatment could cause the above reactions, including bacterial test positive, and some male subjects may be more susceptible.


Gastrointestinal Haemorrhage, International Normalised Ratio Increased, Anaemia, Overdose
A 86-year-old female patient (weight: NA) from FRANCE with the following symptoms/conditions: NA started Tardyferon treatment (dosage: Unk Mg, Unk) on Jan 07, 2011. Soon after starting Tardyferon treatment, the subject experienced various side effects, including:
  • Gastrointestinal Haemorrhage
  • International Normalised Ratio Increased
  • Anaemia
  • Overdose
Concurrently used drugs:
  • Beclomethasone (Unk)
  • Physiotens (1 Df, 1x/day)
  • Aldactone (Unk Mg, Unk)
  • Repaglinide (Unk)
  • Previscan (0.5 Df, 1x/day)
  • Ikorel (10 Mg, 2x/day)
  • Lasix (40 Mg, 1x/day)
  • Ferrous Sulfate (Unk)
The patient was hospitalized. This finding indicates that some female patients could be more vulnerable to Tardyferon.

Condition Aggravated, Premature Labour, Oedema Peripheral, Hypotension, Proteinuria
A female patient from FRANCE (weight: NA) experienced symptoms, such as: anaemia and was treated with Tardyferon(dosage: NA). The treatment was initiated on NS. After that a consumer reported the following side effect(s):
  • Condition Aggravated
  • Premature Labour
  • Oedema Peripheral
  • Hypotension
  • Proteinuria
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Tardyferon efficacy:
  • Risperdal
  • Proctolog
  • Risperdal
  • Risperdal
  • Speciafoldine
  • Risperdal
  • Femibion


Multi-organ Failure, Metabolic Acidosis, Hepatitis Cholestatic, Hypertriglyceridaemia, Cholelithiasis, Lymphoma, Hypoglobulinaemia, Diarrhoea, Altered State Of Consciousness
In this report, Tardyferon /sch/ (iron, Ferrous Sulfate) was administered for the following condition: NA.A 58-year-old male consumer from FRANCE (weight: NA) started Tardyferon /sch/ (iron, Ferrous Sulfate) treatment (dosage: NA) on Mar 01, 2004.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Multi-organ Failure
  • Metabolic Acidosis
  • Hepatitis Cholestatic
  • Hypertriglyceridaemia
  • Cholelithiasis
  • Lymphoma
  • Hypoglobulinaemia
  • Diarrhoea
  • Altered State Of Consciousness
A possible interaction with other drugs could have contributed to this reaction:
  • Lasix
  • Eprex /unk/ (epoetin Alfa)
  • Cellcept (/d)
  • Neoral (/d)
  • Amikin
  • Vancomycin
  • Ferrous Sulfate Tab
  • Ceftazidime
The patient was hospitalized.Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Tardyferon /sch/ (iron, Ferrous Sulfate) treatment could be related to the listed above side effect(s).

Fall, Femur Fracture
This is a report of the following Tardyferon side effect(s):
  • Fall
  • Femur Fracture
A 80-year-old female patient from SPAIN (weight: NA) presented with the following condition: NA and received a treatment with Tardyferon (dosage: NA) starting: Oct 20, 2010.The following concurrently used drugs could have generated interactions:
  • Torsemide
  • Eutirox
  • Forteo (20 Ug, Unk)
  • Insulin
The patient was hospitalized and became disabled.This report suggests that a Tardyferon treatment could be associated with the listed above side effect(s).

Carotid Artery Thrombosis, Cerebrovascular Accident, Hemiplegia
This Tardyferon report was submitted by a 72-year-old male consumer from FRANCE (weight: NA). The patient was diagnosed with: NA and Tardyferon was administered (dosage: Unk) starting: NS. The consumer developed a set of symptoms:
  • Carotid Artery Thrombosis
  • Cerebrovascular Accident
  • Hemiplegia
Other drugs used simultaneously:
  • Mopral (Unk)
  • Cordarone (Unk)
  • Ramipril (Unk)
  • Tenormin (Unk)
  • Tahor (Unk)
  • Kardegic (Unk)
  • Plavix (Unk)
The patient was hospitalized.Those unexpected symptoms could be linked to a Tardyferon treatment, however establishing a potential drug-safety problem requires a more detailed clinical analysis.

Anaemia, Erosive Oesophagitis, Haematemesis, Melaena
This is a report of a possible correlation between Tardyferon use and the following symptoms/side effect(s):
  • Anaemia
  • Erosive Oesophagitis
  • Haematemesis
  • Melaena
which could contribute to an assessment of Tardyferon risk profile.A 89-year-old female consumer from FRANCE (weight: NA) was suffering from iron deficiency anaemia and was treated with Tardyferon (dosage: NA) starting NS.Other concurrent medications:
  • Nexium (2 Unit)
  • Atorvastatin Calcium (1 Unit)
  • Amlodipine (1 Unit)
  • Mepronizine
  • Plavix (Unk)
The patient was hospitalized.

Anaemia, Muscle Haemorrhage, Renal Failure Acute
A 80-year-old female patient from FRANCE (weight: NA) presented with the following symptoms: NA and after a treatment with Tardyferon (dosage: Unk) experienced the following side effect(s):
  • Anaemia
  • Muscle Haemorrhage
  • Renal Failure Acute
The treatment was started on Dec 24, 2006. Tardyferon was used in combination with the following drugs:
  • Previscan
  • Previscan
  • Lovenox
  • Plavix
  • Plavix
  • Plavix
  • Plavix
  • Heparin Choay (Unk)
This report could alert potential Tardyferon consumers.

Anaemia, Muscle Haemorrhage, Renal Failure Acute
In this report, a 80-year-old female patient from FRANCE (weight: NA) was affected by a possible Tardyferon side effect.The patient was diagnosed with NA. After a treatment with Tardyferon (dosage: Unk, start date: Dec 18, 2006), the patient experienced the following side effect(s):
  • Anaemia
  • Muscle Haemorrhage
  • Renal Failure Acute
The following simultaneously used drugs could have led to this reaction:
  • Previscan
  • Lovenox
  • Plavix
The findings here stress that side effects should be taken into consideration when evaluating a Tardyferon treatment.

Agitation, Biopsy Prostate, Blood Glucose Abnormal, Cerebral Atrophy, Confusional State, Depressed Level Of Consciousness, Eating Disorder, Headache, Hypertension
This is a report of a 68-year-old male patient from FRANCE (weight: NA), who used Tardyferon (dosage: NA) for a treatment of NA. After starting a treatment on NS, the patient experienced the following side effect(s):
  • Agitation
  • Biopsy Prostate
  • Blood Glucose Abnormal
  • Cerebral Atrophy
  • Confusional State
  • Depressed Level Of Consciousness
  • Eating Disorder
  • Headache
  • Hypertension
The following drugs could possibly have interacted with the Tardyferon treatment
  • Valium
  • Calcidia
  • Eurobiol
  • Lescol (40 Mg, Qd)
  • Lasilix (500 Mg, Qd)
  • Hexaquine (1 Df, Qd)
  • Un-alfa (4 Df/week)
  • Celectol (200 Mg, Qd)
The patient was hospitalized.Taken together, these observations suggest that a Tardyferon treatment could be related to side effect(s), such as Agitation, Biopsy Prostate, Blood Glucose Abnormal, Cerebral Atrophy, Confusional State, Depressed Level Of Consciousness, Eating Disorder, Headache, Hypertension.

Encephalopathy, Headache, Hypertension
This death side effect was reported by a consumer or non-health professional from FRANCE. A 68-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Tardyferon (dosage: NA), which was started on NS. Concurrently used drugs:
  • Valium
  • Calcidia
  • Eurobiol
  • Lescol (40 Mg, Qd)
  • Lasilix (500 Mg, Qd)
  • Hexaquine (1 Df, Qd)
  • Un-alfa (4 Df/week)
  • Celectol (200 Mg, Qd)
When starting to take Tardyferon the consumer reported the following symptoms:
  • Encephalopathy
  • Headache
  • Hypertension
The patient was hospitalized. These side effects may potentially be related to Tardyferon.

Dermatitis Bullous, Oedema Peripheral, Purpura, Vascular Purpura
This is a Tardyferon side effect report of a 58-year-old male patient (weight:NA) from FRANCE, suffering from the following symptoms/conditions: NA, who was treated with Tardyferon (dosage:NA, start time: Jun 21, 2005), combined with:
  • Neorecormon (3000 Iu/week)
  • Sotalol Hcl
  • Bipreterax
  • Duragesic-100
  • Zometa (1 Df, Once/single)
, and developed a serious reaction and a dermatitis bullous side effect. The patient presented with:
  • Dermatitis Bullous
  • Oedema Peripheral
  • Purpura
  • Vascular Purpura
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Tardyferon treatment in male patients suffering from NA, resulting in dermatitis bullous.

Acute Pulmonary Oedema, Blood Chloride Decreased, Blood Pressure Diastolic Decreased, Blood Pressure Systolic Increased, Cardiac Murmur, Cardiomegaly, Disorientation, Disturbance In Attention
This report suggests a potential Tardyferon acute pulmonary oedema side effect(s) that can have serious consequences. A 93-year-old female patient from (weight:NA) was diagnosed with the following health condition(s): NA and used Tardyferon (dosage: 1 Df, Bid) starting Oct 16, 2004. Soon after starting Tardyferon the patient began experiencing various side effects, including:
  • Acute Pulmonary Oedema
  • Blood Chloride Decreased
  • Blood Pressure Diastolic Decreased
  • Blood Pressure Systolic Increased
  • Cardiac Murmur
  • Cardiomegaly
  • Disorientation
  • Disturbance In Attention
Drugs used concurrently:
  • Kardegic /fra/ (1 Df, Qd)
  • Calciparine
  • Lasilix (20 Mg, Qd)
  • Seropram (20 Mg, Qd)
  • Temesta
  • Imovane
  • Monicor L.p.
  • Vastarel ^biopharma^ (35 Mg, Bid)
The patient was hospitalized. Although Tardyferon demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as acute pulmonary oedema, may still occur.



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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    More About Tardyferon

    Side Effects reported to FDA: 16

    Tardyferon safety alerts: No

    Reported deaths: 5

    Reported hospitalizations: 8

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