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Fozitec adverse events reported to FDA.

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Summary

FDA Adverse Reports: 12. View All

Fozitec FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 11

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Often additional risks of using a medication, such as Fozitec, 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 Fozitec users, Learn more about unwanted side effects & find ways to reduce them. Browse Fozitec Adverse Reports reported to FDA and participate in Fozitec discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Fozitec. 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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Fozitec Adverse Effect Reports (FDA)

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6267089-9 | Acute Pulmonary Oedema, Angina Pectoris, Arrhythmia, Atrioventricular Block, Bronchopneumonia, Cardiogenic Shock, Hyperkalaemia, Renal Failure Acute
on Jul 03, 2009 Male patient from GERMANY , 72 years of age, was diagnosed with hypokalaemia and was treated with Fozitec (View Usage). Patient experienced the following unwanted or unexpected effects: acute pulmonary oedema, angina pectoris, arrhythmia (What is arrhythmia?), atrioventricular block, bronchopneumonia, cardiogenic shock, hyperkalaemia, renal failure acute. Fozitec dosage: . During the same period patient was treated with KALEORID (Start Date: 9 Or 10apr08. Stopped Date:14 Or 15apr08) (View Kaleorid Review and Kaleorid Label ), ALDACTONE (Start Date: Early Apr08.) (View Aldactone Review and Aldactone Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), KREDEX (View Kredex Review and Kredex Label ), LASIX (View Lasix Review and Lasix Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), SOLUPRED (View Solupred Review and Solupred Label ), AUGMENTIN (View Augmentin Review and Augmentin Label ). Patient was hospitalized.

5977810-2 | Cardiac Failure, Renal Failure Acute, Rhabdomyolysis
Patient was taking Fozitec (View Usage). Patient had the following side effects: cardiac failure, renal failure acute, rhabdomyolysis on Nov 27, 2008 from FRANCE Additional patient health information: Male patient , 75 years of age, . Fozitec dosage: . During the same period patient was treated with PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LASIX (View Lasix Review and Lasix Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PREVISCAN (View Previscan Review and Previscan Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), MOPRAL (View Mopral Review and Mopral Label ), AMLOD (View Amlod Review and Amlod Label ). Patient was hospitalized.

5735347-X | Cardiac Failure, Renal Failure Acute, Rhabdomyolysis
Adverse event was reported on May 06, 2008 by a Male patient taking Fozitec (View Usage) (Dosage: ) . Location: GERMANY , 75 years of age, After Fozitec was administered, patient had the following side effects: cardiac failure, renal failure acute, rhabdomyolysis. During the same period patient was treated with PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LASILIX (View Lasilix Review and Lasilix Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PREVISCAN (View Previscan Review and Previscan Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), AMLOR (View Amlor Review and Amlor Label ). Patient was hospitalized.

5720757-7 | Pruritus, Purpura, Rash Maculo-papular
on Apr 18, 2008 Female patient from GERMANY , 82 years of age, was treated with Fozitec (View Usage). Patient experienced the following unwanted or unexpected effects: pruritus, purpura, rash maculo-papular. Fozitec dosage: . During the same period patient was treated with ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), CARBOCISTEINE (View Carbocisteine Review and Carbocisteine Label ), ASPIRIN (160 Mg,powder For Oral Solution) (View Aspirin Review and Aspirin Label ), ADANCOR (View Adancor Review and Adancor Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), EUPRESSYL (View Eupressyl Review and Eupressyl Label ). Patient was hospitalized.


5593603-2 | Altered State Of Consciousness, Disorientation, Hypoglycaemia, Renal Failure Acute
on Jan 11, 2008 Female patient from GERMANY , 86 years of age, was diagnosed with diabetes mellitus, urinary tract infection (What is urinary tract infection?) and was treated with Fozitec (View Usage). Patient had the following side effects: altered state of consciousness, disorientation, hypoglycaemia, renal failure acute. Fozitec dosage: . During the same period patient was treated with DIAMICRON (View Diamicron Review and Diamicron Label ), LASIX (Formulation-tablet) (View Lasix Review and Lasix Label ), NOOTROPYL (Formulation-tablet) (View Nootropyl Review and Nootropyl Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ). Patient was hospitalized.

5566267-1 | Altered State Of Consciousness, Disorientation, Hypoglycaemia, Renal Failure Acute
Patient was taking Fozitec (View Usage). After Fozitec was administered, patient had the following side effects: altered state of consciousness, disorientation, hypoglycaemia, renal failure acute on Dec 12, 2007 from GERMANY Additional patient health information: Female patient , 86 years of age, was diagnosed with diabetes mellitus, urinary tract infection (What is urinary tract infection?) and. Fozitec dosage: . During the same period patient was treated with DIAMICRON (View Diamicron Review and Diamicron Label ), LASIX (Formulation-tablet) (View Lasix Review and Lasix Label ), NOOTROPYL (Formulation-tablet) (View Nootropyl Review and Nootropyl Label ), CIFLOX (View Ciflox Review and Ciflox Label ). Patient was hospitalized.

5290620-7 | Renal Failure Acute
Adverse event was reported on Apr 04, 2007 by a Female patient taking Fozitec (View Usage) (Dosage: ) . Location: GERMANY , 95 years of age, Patient experienced the following unwanted or unexpected effects: renal failure acute. During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), COLCHIMAX (View Colchimax Review and Colchimax Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LASIX (View Lasix Review and Lasix Label ), AVANDIA (View Avandia Review and Avandia Label ), ADANCOR (View Adancor Review and Adancor Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ).

5164545-1 | Bradycardia, Electrocardiogram Qt Prolonged, Torsade De Pointes, Ventricular Extrasystoles
on Nov 20, 2006 Female patient from UNITED STATES , 79 years of age, was treated with Fozitec (View Usage). Patient had the following side effects: bradycardia, electrocardiogram qt prolonged, torsade de pointes, ventricular extrasystoles. Fozitec dosage: . During the same period patient was treated with SOPROL (View Soprol Review and Soprol Label ), CORDARONE (View Cordarone Review and Cordarone Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

5163262-1 | Hyponatraemia, Orthostatic Hypotension
on Nov 20, 2006 Male patient from FRANCE , 87 years of age, was diagnosed with hypertension, dysthymic disorder, arrhythmia (What is arrhythmia?), benign prostatic hyperplasia and was treated with Fozitec (View Usage). After Fozitec was administered, patient had the following side effects: hyponatraemia, orthostatic hypotension. Fozitec dosage: 20 Mg Until 19-aug-2006, 10 Mg- 19 Aug 2006 To 31 Aug 2006; 20 Mg 05 Sep 2006 Onwards. During the same period patient was treated with FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE (View Fosinopril Sodium And Hydrochlorothiazide Review and Fosinopril Sodium And Hydrochlorothiazide Label ), BURINEX (View Burinex Review and Burinex Label ), IXEL (View Ixel Review and Ixel Label ), LASIX (View Lasix Review and Lasix Label ), FLECAINIDE ACETATE (View Flecainide Acetate Review and Flecainide Acetate Label ), PERMIXON (View Permixon Review and Permixon Label ), OMIX (View Omix Review and Omix Label ), PROSCAR (View Proscar Review and Proscar Label ). Patient was hospitalized.

5059349-4 | Dermatitis Bullous, Purpura, Rash Pustular, Renal Failure, Skin Necrosis
Patient was taking Fozitec (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis bullous, purpura, rash pustular, renal failure, skin necrosis on Jun 06, 2006 from FRANCE Additional patient health information: Male patient , 72 years of age, . Fozitec dosage: . During the same period patient was treated with GABAPENTIN (View Gabapentin Review and Gabapentin Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), LASILIX (View Lasilix Review and Lasilix Label ), PERMIXON (View Permixon Review and Permixon Label ), VITAMIN B1 + B6 (View Vitamin B1 + B6 Review and Vitamin B1 + B6 Label ). Patient was hospitalized.

5026351-8 | Dermatitis Bullous, Purpura, Rash Pustular, Renal Failure, Skin Necrosis
Adverse event was reported on Jun 06, 2006 by a Male patient taking Fozitec (View Usage) (Dosage: ) . Location: FRANCE , 72 years of age, Patient had the following side effects: dermatitis bullous, purpura, rash pustular, renal failure, skin necrosis. During the same period patient was treated with GABAPENTIN (View Gabapentin Review and Gabapentin Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), LASILIX (View Lasilix Review and Lasilix Label ), PERMIXON (View Permixon Review and Permixon Label ), VITAMIN B1 + B6 (View Vitamin B1 + B6 Review and Vitamin B1 + B6 Label ). Patient was hospitalized.

4574189-8 | Hyperkalaemia, Hyponatraemia, Malaise, Vertigo
on Jan 31, 2005 Male patient from , 68 years of age, was treated with Fozitec (View Usage). After Fozitec was administered, patient had the following side effects: hyperkalaemia, hyponatraemia, malaise, vertigo. Fozitec dosage: . During the same period patient was treated with APROVEL TABS (View Aprovel Tabs Review and Aprovel Tabs Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), AMLOR (View Amlor Review and Amlor Label ), MEDIATENSYL (View Mediatensyl Review and Mediatensyl Label ), TAHOR (View Tahor Review and Tahor Label ), NOVONORM (View Novonorm Review and Novonorm Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), FLUDEX (View Fludex Review and Fludex Label ). Patient was hospitalized.


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Fozitec Questions, Answers, Feedback and Comments

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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 Fozitec 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 Fozitec quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fozitec 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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Fozitec Reactions
Acute Pulmonary Oedema
Altered State Of Consciousness
Angina Pectoris
ArrhythmiaWhat is Arrhythmia?
Atrioventricular Block
Bradycardia
Bronchopneumonia
Cardiac Failure
Cardiogenic Shock
Dermatitis Bullous
Disorientation
Electrocardiogram Qt Prolonged
Hyperkalaemia
Hypoglycaemia
Hyponatraemia
Malaise
Orthostatic Hypotension
Pruritus
Purpura
Rash Maculo-papular
Rash Pustular
Renal Failure
Renal Failure Acute
Rhabdomyolysis
Skin Necrosis
Torsade De Pointes
Ventricular Extrasystoles
Vertigo
Fozitec 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 Fozitec 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!