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Black Stools (6)
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Tardyferon adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Tardyferon FDA safety alerts: No

Reported deaths: 5

Reported hospitalizations: 6

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1Black Stools
2Stomac Pain
3Itching
4The Dosage Of Tardyferon B9
5Weight Gain
6Diarrhea
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Often additional risks of using a medication, such as Tardyferon, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Tardyferon users, Learn more about unwanted side effects & find ways to reduce them. Browse Tardyferon Adverse Reports reported to FDA and participate in Tardyferon discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Tardyferon. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Tardyferon Adverse Effect Reports (FDA)

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5557410-9 | Carotid Artery Thrombosis, Cerebrovascular Accident, Hemiplegia
on Dec 03, 2007 Male patient from FRANCE , 72 years of age, was treated with Tardyferon (View Usage). Patient experienced the following unwanted or unexpected effects: carotid artery thrombosis, cerebrovascular accident, hemiplegia. Tardyferon dosage: Unk. During the same period patient was treated with MOPRAL (Unk) (View Mopral Review and Mopral Label ), CORDARONE (Unk) (View Cordarone Review and Cordarone Label ), RAMIPRIL (Unk) (View Ramipril Review and Ramipril Label ), TENORMIN (Unk) (View Tenormin Review and Tenormin Label ), TAHOR (Unk) (View Tahor Review and Tahor Label ), KARDEGIC (Unk) (View Kardegic Review and Kardegic Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ). Patient was hospitalized.

5378806-4 | Anaemia, Erosive Oesophagitis, Haematemesis, Melaena
Patient was taking Tardyferon (View Usage). Patient had the following side effects: anaemia, erosive oesophagitis, haematemesis, melaena on Jun 22, 2007 from FRANCE Additional patient health information: Female patient , 89 years of age, was diagnosed with iron deficiency anaemia, essential hypertension, sleep disorder (What is sleep disorder?), ischaemic cardiomyopathy and. Tardyferon dosage: . During the same period patient was treated with NEXIUM (2 Unit) (View Nexium Review and Nexium Label ), ATORVASTATIN CALCIUM (1 Unit) (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), AMLODIPINE (1 Unit) (View Amlodipine Review and Amlodipine Label ), MEPRONIZINE (View Mepronizine Review and Mepronizine Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ). Patient was hospitalized.

5295122-X | Anaemia, Muscle Haemorrhage, Renal Failure Acute
Adverse event was reported on Apr 02, 2007 by a Female patient taking Tardyferon (View Usage) (Dosage: Unk) was diagnosed with heart valve replacement, thrombosis prophylaxis and. Location: FRANCE , 80 years of age, After Tardyferon was administered, patient had the following side effects: anaemia, muscle haemorrhage, renal failure acute. During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ), LOVENOX (View Lovenox Review and Lovenox Label ), PLAVIX (View Plavix Review and Plavix Label ), HEPARIN CHOAY (Unk) (View Heparin Choay Review and Heparin Choay Label ).

5244537-4 | Anaemia, Muscle Haemorrhage, Renal Failure Acute
on Feb 12, 2007 Female patient from FRANCE , 80 years of age, was diagnosed with heart valve replacement, thrombosis prophylaxis and was treated with Tardyferon (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, muscle haemorrhage, renal failure acute. Tardyferon dosage: Unk. During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ), LOVENOX (View Lovenox Review and Lovenox Label ), PLAVIX (View Plavix Review and Plavix Label ).


4948920-3 | Agitation, Biopsy Prostate, Blood Glucose Abnormal, Cerebral Atrophy, Confusional State, Depressed Level Of Consciousness, Eating Disorder, Headache, Hypertension
on Dec 23, 2005 Male patient from FRANCE , 68 years of age, weighting 149.9 lb, was diagnosed with renal failure, essential hypertension and was treated with Tardyferon (View Usage). Patient had the following side effects: agitation, biopsy prostate, blood glucose abnormal, cerebral atrophy, confusional state, depressed level of consciousness, eating disorder (What is eating disorder?), headache (What is headache?), hypertension. Tardyferon dosage: . During the same period patient was treated with VALIUM (View Valium Review and Valium Label ), CALCIDIA (View Calcidia Review and Calcidia Label ), EUROBIOL (View Eurobiol Review and Eurobiol Label ), LESCOL (40 Mg, Qd) (View Lescol Review and Lescol Label ), LASILIX (500 Mg, Qd) (View Lasilix Review and Lasilix Label ), HEXAQUINE (1 Df, Qd) (View Hexaquine Review and Hexaquine Label ), UN ALFA (4 Df/week) (View Un-alfa Review and Un-alfa Label ), CELECTOL (200 Mg, Qd) (View Celectol Review and Celectol Label ). Patient was hospitalized.

4867224-0 | Encephalopathy, Headache, Hypertension
Patient was taking Tardyferon (View Usage). After Tardyferon was administered, patient had the following side effects: encephalopathy, headache (What is headache?), hypertension on Dec 23, 2005 from FRANCE Additional patient health information: Male patient , 68 years of age, weighting 149.9 lb, was diagnosed with renal failure, essential hypertension and. Tardyferon dosage: . During the same period patient was treated with VALIUM (View Valium Review and Valium Label ), CALCIDIA (View Calcidia Review and Calcidia Label ), EUROBIOL (View Eurobiol Review and Eurobiol Label ), LESCOL (40 Mg, Qd) (View Lescol Review and Lescol Label ), LASILIX (500 Mg, Qd) (View Lasilix Review and Lasilix Label ), HEXAQUINE (1 Df, Qd) (View Hexaquine Review and Hexaquine Label ), UN ALFA (4 Df/week) (View Un-alfa Review and Un-alfa Label ), CELECTOL (200 Mg, Qd) (View Celectol Review and Celectol Label ). Patient was hospitalized.

4766234-1 | Dermatitis Bullous, Oedema Peripheral, Purpura, Vascular Purpura
Adverse event was reported on Sep 05, 2005 by a Male patient taking Tardyferon (View Usage) (Dosage: ) . Location: FRANCE , 58 years of age, Patient experienced the following unwanted or unexpected effects: dermatitis bullous, oedema peripheral, purpura, vascular purpura. During the same period patient was treated with NEORECORMON (3000 Iu/week) (View Neorecormon Review and Neorecormon Label ), SOTALOL HCL (View Sotalol Hcl Review and Sotalol Hcl Label ), BIPRETERAX (View Bipreterax Review and Bipreterax Label ), DURAGESIC 100 (View Duragesic-100 Review and Duragesic-100 Label ), ZOMETA (1 Df, Once/single) (View Zometa Review and Zometa Label ). Patient was hospitalized.

4585705-4 | Acute Pulmonary Oedema, Blood Chloride Decreased, Blood Pressure Diastolic Decreased, Blood Pressure Systolic Increased, Cardiac Murmur, Cardiomegaly, Disorientation, Disturbance In Attention
on Nov 26, 2004 Female patient from , 93 years of age, was treated with Tardyferon (View Usage). Patient had the following side effects: acute pulmonary oedema, blood chloride decreased, blood pressure diastolic decreased, blood pressure systolic increased, cardiac murmur, cardiomegaly, disorientation, disturbance in attention. Tardyferon dosage: 1 Df, Bid. During the same period patient was treated with KARDEGIC /FRA/ (1 Df, Qd) (View Kardegic /fra/ Review and Kardegic /fra/ Label ), CALCIPARINE (View Calciparine Review and Calciparine Label ), LASILIX (20 Mg, Qd) (View Lasilix Review and Lasilix Label ), SEROPRAM (20 Mg, Qd) (View Seropram Review and Seropram Label ), TEMESTA (View Temesta Review and Temesta Label ), IMOVANE (View Imovane Review and Imovane Label ), MONICOR L.P. (View Monicor L.p. Review and Monicor L.p. Label ), VASTAREL ^BIOPHARMA^ (35 Mg, Bid) (View Vastarel ^biopharma^ Review and Vastarel ^biopharma^ Label ). Patient was hospitalized.


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Tardyferon Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

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5:55am on Tuesday, November 3rd, 2009

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Anonymous   Location unknown

1:31pm on Friday, October 16th, 2009

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Tardyferon risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Tardyferon quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tardyferon use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Tardyferon Reactions
Acute Pulmonary Oedema
Agitation
Anaemia
Biopsy Prostate
Blood Chloride Decreased
Blood Glucose Abnormal
Blood Pressure Diastolic Decreased
Blood Pressure Systolic Increased
Cardiac Murmur
Cardiomegaly
Carotid Artery Thrombosis
Cerebral Atrophy
Cerebrovascular Accident
Confusional State
Death
Depressed Level Of Consciousness
Dermatitis Bullous
Disorientation
Disturbance In Attention
Eating DisorderWhat is Eating disorder?
Encephalopathy
Erosive Oesophagitis
Haematemesis
HeadacheWhat is Headache?
Hemiplegia
Hypertension
Melaena
Muscle Haemorrhage
Oedema Peripheral
Renal Failure Acute
Tardyferon Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Tardyferon adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!