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Tazicef adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Tazicef FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 3

Tazicef Dosage, Warnings, Usage.

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

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5133046-9 | Klebsiella Infection, Nosocomial Infection, Peritonitis
on Mar 24, 2006 Male patient from TAIWAN, PROVINCE OF CHINA , 45 years of age, was diagnosed with peritonitis and was treated with Tazicef (View Usage). Patient experienced the following unwanted or unexpected effects: klebsiella infection, nosocomial infection, peritonitis. Tazicef dosage: 1 Gm; Parn. During the same period patient was treated with GENTAMICIN (View Gentamicin Review and Gentamicin Label ), TEICOPLANIN (TEICOPLANIN) (400 Mg; Parn) (View Teicoplanin (teicoplanin) Review and Teicoplanin (teicoplanin) Label ).

5107198-0 | Endophthalmitis, Eye Pain, Staphylococcal Infection
Patient was taking Tazicef (View Usage). Patient had the following side effects: endophthalmitis, eye pain, staphylococcal infection (What is staphylococcal infection?) on Aug 29, 2006 from UNITED STATES Additional patient health information: Female patient , 78 years of age, was diagnosed with endophthalmitis and. Tazicef dosage: 2 Mg; Con. During the same period patient was treated with VANCOMYCIN HCL (Con) (View Vancomycin Hcl Review and Vancomycin Hcl Label ). Patient was hospitalized.

5101376-2 | Agitation, Confusional State, Myoclonus, Neurological Symptom, Status Epilepticus
Adverse event was reported on Aug 15, 2006 by a Male patient taking Tazicef (View Usage) (Dosage: 2 Gm; Unk;iv) was diagnosed with pneumonia (What is pneumonia?) and. Location: SPAIN , 64 years of age, After Tazicef was administered, patient had the following side effects: agitation, confusional state, myoclonus, neurological symptom, status epilepticus.

5100790-9 | Confusional State, Myoclonus, Neurological Symptom, Status Epilepticus
on Aug 15, 2006 Male patient from SPAIN , 38 years of age, was diagnosed with pneumonia (What is pneumonia?) and was treated with Tazicef (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, myoclonus, neurological symptom, status epilepticus. Tazicef dosage: 2 Gm, Iv.


5093591-1 | Blood Creatinine Increased, Coma, Confusional State, Disorientation, Lethargy, Mental Status Changes, Metabolic Disorder, Myoclonus
on Aug 16, 2006 Male patient from UNITED STATES , 77 years of age, was diagnosed with meningitis (What is meningitis?) and was treated with Tazicef (View Usage). Patient had the following side effects: blood creatinine increased, coma, confusional state, disorientation, lethargy, mental status changes, metabolic disorder (What is metabolic disorder?), myoclonus. Tazicef dosage: 2 Gm;every 8 Hr;iv. During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), HYDROCHLORIDE (View Hydrochloride Review and Hydrochloride Label ), GENTAMICIN SULFATE (View Gentamicin Sulfate Review and Gentamicin Sulfate Label ).

5088363-8 | Anxiety, Status Epilepticus
Patient was taking Tazicef (View Usage). After Tazicef was administered, patient had the following side effects: anxiety (What is anxiety?), status epilepticus on Aug 11, 2006 from ITALY Additional patient health information: Female patient , 72 years of age, was diagnosed with peritonitis and. Tazicef dosage: 4 Gm; Every Day; Unk. During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ).

5076816-8 | Anaphylactic Shock, Blood Creatinine Decreased, Blood Urea Increased, Bundle Branch Block Left, Culture Urine Positive, Dermatitis Contact, Fall, Haematuria, Myocardial Infarction
Adverse event was reported on Jul 04, 2005 by a Female patient taking Tazicef (View Usage) (Dosage: 1 Gm;once;iv) was diagnosed with prophylaxis and. Location: SRI LANKA , 72 years of age, Patient experienced the following unwanted or unexpected effects: anaphylactic shock, blood creatinine decreased, blood urea increased, bundle branch block left, culture urine positive, dermatitis contact, fall (What is fall?), haematuria, myocardial infarction. Patient was hospitalized.

4619526-0 | Staphylococcal Infection
on Mar 01, 2005 Female patient from , 78 years of age, was diagnosed with endophthalmitis and was treated with Tazicef (View Usage). Patient had the following side effects: staphylococcal infection (What is staphylococcal infection?). Tazicef dosage: 2 Mg; Conjunctival. During the same period patient was treated with VANCOMYCIN HCL (Conjunctival) (View Vancomycin Hcl Review and Vancomycin Hcl Label ). Patient was hospitalized.


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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 Tazicef 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 Tazicef quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tazicef 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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Tazicef Reactions
Agitation
Anaphylactic Shock
AnxietyWhat is Anxiety?
Blood Creatinine Decreased
Blood Creatinine Increased
Blood Urea Increased
Bundle Branch Block Left
Coma
Confusional State
Culture Urine Positive
Dermatitis Contact
Disorientation
Endophthalmitis
Eye Pain
FallWhat is Fall?
Haematuria
Klebsiella Infection
Lethargy
Mental Status Changes
Metabolic DisorderWhat is Metabolic disorder?
Myocardial Infarction
Myoclonus
Neurological Symptom
Nosocomial Infection
Peritonitis
Staphylococcal InfectionWhat is Staphylococcal infection?
Status Epilepticus
Tazicef 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 Tazicef 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!