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Summary

FDA Adverse Reports: 136. View All

Zinacef FDA safety alerts: No

Reported deaths: 15

Reported hospitalizations: 58

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

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6945766-1 | Anaphylactic Shock
on Aug 18, 2010 Female patient from GREECE , 62 years of age, was diagnosed with prophylaxis and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock. Zinacef dosage: . During the same period patient was treated with APOTEL (View Apotel Review and Apotel Label ). Patient was hospitalized.

6764203-3 | Anaphylactic Shock, Bronchospasm, Circulatory Collapse, Endotracheal Intubation, Face Oedema, Hypotension, Laryngeal Oedema
Patient was taking Zinacef (View Usage). Patient had the following side effects: anaphylactic shock, bronchospasm, circulatory collapse, endotracheal intubation, face oedema, hypotension, laryngeal oedema on Jun 02, 2010 from SWITZERLAND Additional patient health information: Male patient , weighting 165.3 lb, . Zinacef dosage: . Patient was hospitalized.

6664155-0 | Anaphylactic Shock
Adverse event was reported on Mar 26, 2010 by a Female patient taking Zinacef (View Usage) (Dosage: ) was diagnosed with prophylaxis and. Location: GREECE , 62 years of age, After Zinacef was administered, patient had the following side effects: anaphylactic shock. During the same period patient was treated with APOTEL (View Apotel Review and Apotel Label ). Patient was hospitalized.

6430671-X | Body Temperature Increased, Chills, Cholestatic Liver Injury, Enanthema, Erythema, Faeces Pale, Hepatocellular Injury, Hyperbilirubinaemia
on Oct 29, 2009 Female patient from SWITZERLAND , weighting 185.2 lb, was diagnosed with prophylaxis and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: body temperature increased, chills, cholestatic liver injury, enanthema, erythema, faeces pale, hepatocellular injury, hyperbilirubinaemia. Zinacef dosage: . During the same period patient was treated with NEXIUM (20mg Per Day) (View Nexium Review and Nexium Label ), IBRUPROFEN (600mg Three Times Per Day) (View Ibruprofen Review and Ibruprofen Label ).


6372126-7 | Pemphigus, Pharyngitis Bacterial
on Sep 07, 2009 Male patient from ITALY , 14 years of age, was treated with Zinacef (View Usage). Patient had the following side effects: pemphigus (What is pemphigus?), pharyngitis bacterial. Zinacef dosage: Oral.

6341100-9 | C-reactive Protein Increased, Eosinophilia, Leukocytosis, Neutrophil Count Increased, Pruritus, Pyrexia, Rash Erythematous, Rash Pustular
Patient was taking Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: c-reactive protein increased, eosinophilia, leukocytosis, neutrophil count increased, pruritus, pyrexia, rash erythematous, rash pustular on Aug 24, 2009 from GREECE Additional patient health information: Female patient , 56 years of age, was diagnosed with skin lesion and. Zinacef dosage: 750mg Three Times Per Day. During the same period patient was treated with DALACIN (600mg Twice Per Day) (View Dalacin Review and Dalacin Label ).

6336495-6 | Arthralgia, Diarrhoea, Feeling Hot, Hospitalisation
Adverse event was reported on Aug 31, 2009 by a Male patient taking Zinacef (View Usage) (Dosage: 1.5g Per Day) was diagnosed with infection prophylaxis, pulmonary embolism (What is pulmonary embolism?), carotid artery stenosis and. Location: GERMANY , 78 years of age, weighting 202.8 lb, Patient experienced the following unwanted or unexpected effects: arthralgia, diarrhoea, feeling hot, hospitalisation. During the same period patient was treated with PANTOZOL (40mg Per Day) (View Pantozol Review and Pantozol Label ), AMPICILLIN AND SULBACTAM (1500mg Per Day) (View Ampicillin And Sulbactam Review and Ampicillin And Sulbactam Label ), FALITHROM (View Falithrom Review and Falithrom Label ), HYDROCHLOROTHIAZIDE (12.5mg Per Day) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), L THYROXIN (100mcg Per Day) (View L-thyroxin Review and L-thyroxin Label ), RAMIPRIL (5mg Per Day) (View Ramipril Review and Ramipril Label ), SIMVASTATIN (20mg Per Day) (View Simvastatin Review and Simvastatin Label ), TAMSULOSIN (.4mg Per Day) (View Tamsulosin Review and Tamsulosin Label ). Patient was hospitalized.

6331068-3 | Dyspnoea, Rash Macular, Rash Pruritic
on Aug 21, 2009 Female patient from POLAND , weighting 68.34 lb, was treated with Zinacef (View Usage). Patient had the following side effects: dyspnoea, rash macular, rash pruritic. Zinacef dosage: 750mg Twice Per Day. During the same period patient was treated with MUCOSOLVAN (View Mucosolvan Review and Mucosolvan Label ), TANTUM VERDE (View Tantum Verde Review and Tantum Verde Label ), APO NAPROXEN (View Apo Naproxen Review and Apo Naproxen Label ). Patient was hospitalized.

6292752-3 | Blood Pressure Increased, Dysgeusia, Dyspnoea, Feeling Hot, Product Quality Issue
on Jul 24, 2009 Female patient from POLAND , weighting 141.1 lb, was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: blood pressure increased, dysgeusia, dyspnoea, feeling hot, product quality issue. Zinacef dosage: 1500mg Twice Per Day. During the same period patient was treated with HYDROXYZINE (20mg Per Day) (View Hydroxyzine Review and Hydroxyzine Label ), METAMIZOL SODIUM (5ml Twice Per Day) (View Metamizol Sodium Review and Metamizol Sodium Label ).

6254644-5 | Coma, Loss Of Consciousness, Pyrexia, Transmission Of An Infectious Agent Via A Medicinal Product
Patient was taking Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: coma, loss of consciousness, pyrexia, transmission of an infectious agent via a medicinal product on Jun 20, 2009 from PAKISTAN Additional patient health information: Male patient , child 12 years of age, was diagnosed with hernia repair and. Zinacef dosage: .

6208901-9 | Blood Pressure Increased, Dysgeusia, Dyspnoea, Feeling Hot
Adverse event was reported on May 21, 2009 by a Female patient taking Zinacef (View Usage) (Dosage: 1500mg Twice Per Day) . Location: POLAND , weighting 141.1 lb, Patient had the following side effects: blood pressure increased, dysgeusia, dyspnoea, feeling hot. During the same period patient was treated with HYDROXYZINE (20mg Per Day) (View Hydroxyzine Review and Hydroxyzine Label ), METAMIZOL SODIUM (5ml Twice Per Day) (View Metamizol Sodium Review and Metamizol Sodium Label ).

6179426-4 | Blood Pressure Decreased, Heart Rate Decreased, Hyperhidrosis, Hypotonia, Pulse Abnormal, Syncope, Tachycardia
on Apr 30, 2009 Male patient from POLAND , weighting 231.5 lb, was diagnosed with acute sinusitis and was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: blood pressure decreased, heart rate decreased, hyperhidrosis, hypotonia, pulse abnormal, syncope, tachycardia. Zinacef dosage: .

6115095-7 | Blood Pressure Decreased, Cardiac Arrest, Dyspnoea, Oxygen Saturation Decreased, Syncope
on Mar 05, 2009 Female patient from POLAND , 16 years of age, weighting 127.9 lb, was diagnosed with tracheitis and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, cardiac arrest (What is cardiac arrest?), dyspnoea, oxygen saturation decreased, syncope. Zinacef dosage: .

6113030-9 | Depressed Level Of Consciousness, Pyrexia, Thrombocytopenia
Patient was taking Zinacef (View Usage). Patient had the following side effects: depressed level of consciousness, pyrexia, thrombocytopenia on Mar 05, 2009 from SWEDEN Additional patient health information: Male patient , 89 years of age, was diagnosed with pneumonia (What is pneumonia?), urinary tract infection (What is urinary tract infection?) and. Zinacef dosage: 4.5g Per Day. During the same period patient was treated with ALVEDON (View Alvedon Review and Alvedon Label ), CHLOROMYCETIN (View Chloromycetin Review and Chloromycetin Label ), FURADANTIN (View Furadantin Review and Furadantin Label ), BEHEPAN (View Behepan Review and Behepan Label ), LASIX (View Lasix Review and Lasix Label ), LAKTULOS (View Laktulos Review and Laktulos Label ), OXASCAND (View Oxascand Review and Oxascand Label ), IMDUR (View Imdur Review and Imdur Label ). Patient was hospitalized.

6100086-2 | Melaena
Adverse event was reported on Feb 25, 2009 by a Female patient taking Zinacef (View Usage) (Dosage: ) was diagnosed with urinary tract infection (What is urinary tract infection?) and. Location: MALAYSIA , 81 years of age, After Zinacef was administered, patient had the following side effects: melaena.

6074138-X | Eyelid Oedema, Infection, Oedema Peripheral, Pruritus, Rash
on Feb 05, 2009 Male patient from SWEDEN , 72 years of age, was diagnosed with pneumonia (What is pneumonia?) and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: eyelid oedema, infection (What is infection?), oedema peripheral, pruritus, rash (What is rash?). Zinacef dosage: . During the same period patient was treated with KAVEPENIN (View Kavepenin Review and Kavepenin Label ), SELOKEN (View Seloken Review and Seloken Label ), TROMBYL (View Trombyl Review and Trombyl Label ). Patient was hospitalized.

6013749-4 | Anaphylactic Shock, Dysgeusia, Malaise, Product Quality Issue, Ventricular Fibrillation
on Dec 18, 2008 Female patient from FINLAND , 70 years of age, was treated with Zinacef (View Usage). Patient had the following side effects: anaphylactic shock, dysgeusia, malaise, product quality issue, ventricular fibrillation. Zinacef dosage: . During the same period patient was treated with FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), LIDOCAINE (View Lidocaine Review and Lidocaine Label ), OXYGEN (View Oxygen Review and Oxygen Label ), ATROPINE (View Atropine Review and Atropine Label ), EPINEPHRINE (View Epinephrine Review and Epinephrine Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), KETANEST (View Ketanest Review and Ketanest Label ), PAVULON (View Pavulon Review and Pavulon Label ). Patient was hospitalized.

6013748-2 | Abdominal Pain Upper, Anaphylactic Reaction, Dysgeusia, Hypotension, Loss Of Consciousness, Malaise, Nausea, Product Quality Issue
Patient was taking Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: abdominal pain upper, anaphylactic reaction, dysgeusia, hypotension, loss of consciousness, malaise, nausea (What is nausea?), product quality issue on Dec 18, 2008 from FINLAND Additional patient health information: Male patient , 45 years of age, . Zinacef dosage: . During the same period patient was treated with NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), RENITEC COMP (View Renitec Comp Review and Renitec Comp Label ), OXYCONTIN (20mg Twice Per Day) (View Oxycontin Review and Oxycontin Label ), PARATABS (1g Three Times Per Day) (View Paratabs Review and Paratabs Label ), RIVATRIL (.5mg Four Times Per Day) (View Rivatril Review and Rivatril Label ), TENOX (20mg Per Day) (View Tenox Review and Tenox Label ), CIPRALEX (20mg Per Day) (View Cipralex Review and Cipralex Label ), REMERON (15mg Per Day) (View Remeron Review and Remeron Label ). Patient was hospitalized.

6000091-0 | Anaphylactic Shock, Dysgeusia, Malaise, Product Quality Issue, Ventricular Fibrillation
Adverse event was reported on Dec 04, 2008 by a Female patient taking Zinacef (View Usage) (Dosage: ) . Location: FINLAND , 70 years of age, Patient experienced the following unwanted or unexpected effects: anaphylactic shock, dysgeusia, malaise, product quality issue, ventricular fibrillation. During the same period patient was treated with FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), LIDOCAINE (View Lidocaine Review and Lidocaine Label ), OXYGEN (View Oxygen Review and Oxygen Label ), ATROPINE (View Atropine Review and Atropine Label ), EPINEPHRINE (View Epinephrine Review and Epinephrine Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), KETANEST (View Ketanest Review and Ketanest Label ), PAVULON (View Pavulon Review and Pavulon Label ). Patient was hospitalized.

5990629-1 | Clostridial Infection, Diarrhoea, Gastroenteritis
on Dec 05, 2008 Male patient from FINLAND , 88 years of age, was diagnosed with osteoporosis (What is osteoporosis?), restlessness, pain (What is pain?), atrial fibrillation (What is atrial fibrillation?) and was treated with Zinacef (View Usage). Patient had the following side effects: clostridial infection, diarrhoea, gastroenteritis (What is gastroenteritis?). Zinacef dosage: . During the same period patient was treated with KEFEXIN (750mg Three Times Per Day) (View Kefexin Review and Kefexin Label ), KALCIPOS D (1tab Per Day) (View Kalcipos-d Review and Kalcipos-d Label ), ARICEPT (1tab Per Day) (View Aricept Review and Aricept Label ), HALOPERIDOL (1tab Per Day) (View Haloperidol Review and Haloperidol Label ), OXYTOCIN (2tab Twice Per Day) (View Oxytocin Review and Oxytocin Label ), TIZANIDINE HCL (1tab Three Times Per Day) (View Tizanidine Hcl Review and Tizanidine Hcl Label ), MAREVAN (View Marevan Review and Marevan Label ), ORLOC (1tab Per Day) (View Orloc Review and Orloc Label ).

5987042-X | Abdominal Pain Upper, Anaphylactic Reaction, Dysgeusia, Hypotension, Loss Of Consciousness, Malaise, Nausea, Product Quality Issue
on Dec 04, 2008 Male patient from FINLAND , 45 years of age, was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: abdominal pain upper, anaphylactic reaction, dysgeusia, hypotension, loss of consciousness, malaise, nausea (What is nausea?), product quality issue. Zinacef dosage: . During the same period patient was treated with NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), RENITEC COMP (View Renitec Comp Review and Renitec Comp Label ), OXYCONTIN (20mg Twice Per Day) (View Oxycontin Review and Oxycontin Label ), PARATABS (1g Three Times Per Day) (View Paratabs Review and Paratabs Label ), RIVATRIL (.5mg Four Times Per Day) (View Rivatril Review and Rivatril Label ), TENOX (20mg Per Day) (View Tenox Review and Tenox Label ), CIPRALEX (20mg Per Day) (View Cipralex Review and Cipralex Label ), REMERON (15mg Per Day) (View Remeron Review and Remeron Label ). Patient was hospitalized.

5951829-X | Agranulocytosis, C-reactive Protein Increased, Leukopenia, Neutrophil Count Decreased
Patient was taking Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: agranulocytosis, c-reactive protein increased, leukopenia, neutrophil count decreased on Oct 30, 2008 from FINLAND Additional patient health information: Male patient , 80 years of age, was diagnosed with thrombosis prophylaxis, pain (What is pain?), constipation (What is constipation?) and. Zinacef dosage: 1.5g Three Times Per Day. During the same period patient was treated with TAVANIC (500mg Per Day) (View Tavanic Review and Tavanic Label ), ENOXAPARIN SODIUM (40mg Per Day) (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), MOVICOL (View Movicol Review and Movicol Label ), LAXOBERON (View Laxoberon Review and Laxoberon Label ), ACETAMINOPHEN (1g Three Times Per Day) (View Acetaminophen Review and Acetaminophen Label ), XATRAL (10mg Per Day) (View Xatral Review and Xatral Label ). Patient was hospitalized.

5950222-3 | Anaphylactic Reaction, Blood Pressure Systolic Decreased, Obstructive Airways Disorder, Rash Erythematous
Adverse event was reported on Nov 05, 2008 by a Female patient taking Zinacef (View Usage) (Dosage: 1.5mg Single Dose) was diagnosed with prophylaxis and. Location: FINLAND , 74 years of age, Patient had the following side effects: anaphylactic reaction, blood pressure systolic decreased, obstructive airways disorder, rash erythematous. During the same period patient was treated with METRONIDAZOLE (.5g Single Dose) (View Metronidazole Review and Metronidazole Label ), PROPOFOL (120mg Single Dose) (View Propofol Review and Propofol Label ), FENTANYL (.1mg Single Dose) (View Fentanyl Review and Fentanyl Label ), LIDOCAINE (30mg Single Dose) (View Lidocaine Review and Lidocaine Label ), ROBINUL (.2mg Single Dose) (View Robinul Review and Robinul Label ), ROCURONIUM BROMIDE (40mg Single Dose) (View Rocuronium Bromide Review and Rocuronium Bromide Label ), DIAPAM (5mg Single Dose) (View Diapam Review and Diapam Label ), OMEPRAZOLE (20u Single Dose) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5945201-6 | Agranulocytosis, C-reactive Protein Increased, Leukopenia, Neutrophil Count Decreased
on Oct 30, 2008 Male patient from FINLAND , 80 years of age, was diagnosed with thrombosis prophylaxis, pain (What is pain?), constipation (What is constipation?) and was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: agranulocytosis, c-reactive protein increased, leukopenia, neutrophil count decreased. Zinacef dosage: 1.5g Three Times Per Day. During the same period patient was treated with TAVANIC (500mg Per Day) (View Tavanic Review and Tavanic Label ), ENOXAPARIN SODIUM (40mg Per Day) (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), MOVICOL (View Movicol Review and Movicol Label ), LAXOBERON (View Laxoberon Review and Laxoberon Label ), ACETAMINOPHEN (1g Three Times Per Day) (View Acetaminophen Review and Acetaminophen Label ), XATRAL (10mg Per Day) (View Xatral Review and Xatral Label ). Patient was hospitalized.

5943227-X | Tendon Rupture
on Oct 31, 2008 Male patient from FINLAND , 31 years of age, was diagnosed with pneumonia (What is pneumonia?) and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: tendon rupture. Zinacef dosage: . During the same period patient was treated with AVELOX (View Avelox Review and Avelox Label ).

5920504-X | Chills, Chromaturia, Cyanosis, Pyrexia, Urine Abnormality
Patient was taking Zinacef (View Usage). Patient had the following side effects: chills, chromaturia, cyanosis, pyrexia, urine abnormality on Oct 09, 2008 from PHILIPPINES Additional patient health information: Female patient , child 5 years of age, . Zinacef dosage: . During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

5907480-0 | Chills, Chromaturia, Cyanosis, Urine Abnormality
Adverse event was reported on Sep 26, 2008 by a Female patient taking Zinacef (View Usage) (Dosage: ) . Location: PHILIPPINES , child 5 years of age, After Zinacef was administered, patient had the following side effects: chills, chromaturia, cyanosis, urine abnormality.

5893308-4 | Corneal Deposits, Corneal Opacity, Off Label Use
on Sep 16, 2008 Male patient from IRELAND , 86 years of age, was diagnosed with eye infection (What is eye infection?) and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: corneal deposits, corneal opacity, off label use. Zinacef dosage: .

5886347-0 | Diarrhoea, Inflammation, Pyrexia, Vomiting
on Sep 16, 2008 Female patient from SWITZERLAND , 87 years of age, was treated with Zinacef (View Usage). Patient had the following side effects: diarrhoea, inflammation, pyrexia, vomiting. Zinacef dosage: . During the same period patient was treated with MEFENACID (View Mefenacid Review and Mefenacid Label ), ACULAR (View Acular Review and Acular Label ). Patient was hospitalized.

5884960-8 | Corneal Opacity, Off Label Use
Patient was taking Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: corneal opacity, off label use on Sep 11, 2008 from IRELAND Additional patient health information: Male patient , 73 years of age, was diagnosed with eye infection (What is eye infection?) and. Zinacef dosage: .

5879443-5 | Diarrhoea, Inflammation, Pyrexia, Vomiting
Adverse event was reported on Sep 05, 2008 by a Female patient taking Zinacef (View Usage) (Dosage: ) . Location: SWITZERLAND , 87 years of age, Patient experienced the following unwanted or unexpected effects: diarrhoea, inflammation, pyrexia, vomiting. During the same period patient was treated with MEFENACID (View Mefenacid Review and Mefenacid Label ), ACULAR (View Acular Review and Acular Label ). Patient was hospitalized.

5870633-4 | Anaphylactic Reaction, Angioedema, Anxiety, Skin Discolouration, Vasodilation Procedure
on Aug 29, 2008 Female patient from NETHERLANDS , 25 years of age, was diagnosed with prophylaxis and was treated with Zinacef (View Usage). Patient had the following side effects: anaphylactic reaction, angioedema, anxiety (What is anxiety?), skin discolouration, vasodilation procedure. Zinacef dosage: . During the same period patient was treated with LOPERAMIDE HCL (2mg Twice Per Day) (View Loperamide Hcl Review and Loperamide Hcl Label ), PREDNISOLON (5mg Four Times Per Day) (View Prednisolon Review and Prednisolon Label ), CRANBERRY (View Cranberry Review and Cranberry Label ), FUROSEMIDE (40mg Per Day) (View Furosemide Review and Furosemide Label ), ATENOLOL (50mg Per Day) (View Atenolol Review and Atenolol Label ), DRIDASE (2.5mg Per Day) (View Dridase Review and Dridase Label ), ASCORBIC ACID (500mg Per Day) (View Ascorbic Acid Review and Ascorbic Acid Label ), DEPAKENE (500mg Per Day) (View Depakene Review and Depakene Label ).

5846676-3 | Acute Hepatic Failure, Blister, Gastrointestinal Haemorrhage, Necrosis, Nikolsky's Sign, Renal Failure Acute, Toxic Epidermal Necrolysis
on Aug 06, 2008 Female patient from BELGIUM , 52 years of age, weighting 88.18 lb, was diagnosed with blood culture, escherichia urinary tract infection, prophylaxis, hepatorenal syndrome, vitamin supplementation and was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: acute hepatic failure, blister, gastrointestinal haemorrhage, necrosis, nikolsky's sign, renal failure acute, toxic epidermal necrolysis. Zinacef dosage: 1.5g Twice Per Day. During the same period patient was treated with CLAFORAN (2g Three Times Per Day) (View Claforan Review and Claforan Label ), ZANTAC (50mg Twice Per Day) (View Zantac Review and Zantac Label ), GLYPRESSIN (.5mg Six Times Per Day) (View Glypressin Review and Glypressin Label ), KONAKION (10mg Per Day) (View Konakion Review and Konakion Label ), CERNEVIT 12 (1amp Per Day) (View Cernevit-12 Review and Cernevit-12 Label ), ADDAMEL (1amp Per Day) (View Addamel Review and Addamel Label ), LASIX (60mg Per Day) (View Lasix Review and Lasix Label ), SOLU MEDROL (60mg Per Day) (View Solu-medrol Review and Solu-medrol Label ). Patient was hospitalized.

5841829-2 | Corneal Deposits, Corneal Opacity, Off Label Use
Patient was taking Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: corneal deposits, corneal opacity, off label use on Aug 05, 2008 from IRELAND Additional patient health information: Male patient , 86 years of age, was diagnosed with eye infection (What is eye infection?) and. Zinacef dosage: .

5836859-0 | Pancytopenia
Adverse event was reported on Jul 30, 2008 by a Female patient taking Zinacef (View Usage) (Dosage: 1.5g Three Times Per Day) was diagnosed with pneumonia (What is pneumonia?), blood pressure (What is blood pressure?) and. Location: FINLAND , 90 years of age, Patient had the following side effects: pancytopenia. During the same period patient was treated with ROCEPHIN (2g Per Day) (View Rocephin Review and Rocephin Label ), SOMAC (40mg Per Day) (View Somac Review and Somac Label ), CARDACE (10mg Per Day) (View Cardace Review and Cardace Label ), KALINORM (View Kalinorm Review and Kalinorm Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), ORMOX (View Ormox Review and Ormox Label ), FURESIS (View Furesis Review and Furesis Label ), EMCONCOR (View Emconcor Review and Emconcor Label ).

5835552-8 | Corneal Deposits, Corneal Opacity, Off Label Use
on Aug 01, 2008 Male patient from IRELAND , 86 years of age, was diagnosed with eye infection (What is eye infection?) and was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: corneal deposits, corneal opacity, off label use. Zinacef dosage: .

5835551-6 | Corneal Opacity, Off Label Use
on Aug 01, 2008 Male patient from IRELAND , 73 years of age, was diagnosed with eye infection (What is eye infection?) and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: corneal opacity, off label use. Zinacef dosage: .

5798209-8 | Anaphylactic Reaction, Cerebral Infarction, Convulsion, Dyspnoea, Loss Of Consciousness, Nausea, Oropharyngeal Discomfort
Patient was taking Zinacef (View Usage). Patient had the following side effects: anaphylactic reaction, cerebral infarction, convulsion, dyspnoea, loss of consciousness, nausea (What is nausea?), oropharyngeal discomfort on Jun 27, 2008 from MALAYSIA Additional patient health information: Female patient , 26 years of age, was diagnosed with tonsillitis and. Zinacef dosage: 750mg Three Times Per Day. Patient was hospitalized and became disabled.

5789049-4 | Epigastric Discomfort, Hypotension, Pruritus, Rash Erythematous, Tachycardia
Adverse event was reported on Jun 20, 2008 by a Male patient taking Zinacef (View Usage) (Dosage: ) was diagnosed with prophylaxis, hypotension and. Location: IRELAND , 51 years of age, After Zinacef was administered, patient had the following side effects: epigastric discomfort, hypotension, pruritus, rash erythematous, tachycardia. During the same period patient was treated with GELOFUSINE (View Gelofusine Review and Gelofusine Label ), GELATIN (View Gelatin Review and Gelatin Label ), HYPNOVEL (View Hypnovel Review and Hypnovel Label ), MARCAINE HCL W/ EPINEPHRINE (View Marcaine Hcl W/ Epinephrine Review and Marcaine Hcl W/ Epinephrine Label ), SODIUM LACTATE (View Sodium Lactate Review and Sodium Lactate Label ), ATROPINE (View Atropine Review and Atropine Label ).

5771887-5 | Epigastric Discomfort, Hypotension, Pruritus, Rash Erythematous, Tachycardia
on Jun 05, 2008 Male patient from IRELAND , 51 years of age, was diagnosed with prophylaxis and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: epigastric discomfort, hypotension, pruritus, rash erythematous, tachycardia. Zinacef dosage: . During the same period patient was treated with GELATIN (View Gelatin Review and Gelatin Label ), HYPNOVEL (View Hypnovel Review and Hypnovel Label ), MARCAINE HCL W/ EPINEPHRINE (View Marcaine Hcl W/ Epinephrine Review and Marcaine Hcl W/ Epinephrine Label ).

5749524-5 | Blood Pressure Decreased, Hyperhidrosis, Pulse Abnormal, Syncope, Tachycardia
on May 21, 2008 Male patient from POLAND , 72 years of age, was diagnosed with acute sinusitis and was treated with Zinacef (View Usage). Patient had the following side effects: blood pressure decreased, hyperhidrosis, pulse abnormal, syncope, tachycardia. Zinacef dosage: .

5712867-5 | Blood Pressure Decreased, Heart Rate Decreased, Hyperhidrosis, Hypotonia, Syncope, Tachycardia
Patient was taking Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: blood pressure decreased, heart rate decreased, hyperhidrosis, hypotonia, syncope, tachycardia on Apr 14, 2008 from POLAND Additional patient health information: Male patient , 22 years of age, weighting 231.5 lb, was diagnosed with acute sinusitis and. Zinacef dosage: .

5709654-0 | Hyperhidrosis, Hypotonia, Pulse Pressure Decreased, Syncope, Tachycardia
Adverse event was reported on Apr 14, 2008 by a Male patient taking Zinacef (View Usage) (Dosage: ) . Location: POLAND , 26 years of age, weighting 209.4 lb, Patient experienced the following unwanted or unexpected effects: hyperhidrosis, hypotonia, pulse pressure decreased, syncope, tachycardia.

5707073-4 | Body Temperature Increased, Chills, Disseminated Intravascular Coagulation, Multi-organ Failure
on Mar 11, 2008 Male patient from CHINA , 45 years of age, was treated with Zinacef (View Usage). Patient had the following side effects: body temperature increased, chills, disseminated intravascular coagulation, multi-organ failure. Zinacef dosage: 1.5g Per Day. During the same period patient was treated with QING KAI LING (View Qing Kai Ling Review and Qing Kai Ling Label ). Patient was hospitalized.

5689063-3 | Blood Test Abnormal, Jaundice Cholestatic
on Mar 27, 2008 Female patient from UNITED KINGDOM , 40 years of age, was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: blood test abnormal, jaundice cholestatic. Zinacef dosage: 1.5g Single Dose.

5630596-3 | Cerebral Infarction, Clostridial Infection, Diarrhoea, Enterocolitis
Patient was taking Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral infarction, clostridial infection, diarrhoea, enterocolitis on Feb 11, 2008 from SWEDEN Additional patient health information: Female patient , 78 years of age, was diagnosed with pyelonephritis and. Zinacef dosage: . During the same period patient was treated with CIPROXIN (View Ciproxin Review and Ciproxin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), PEVARYL CREAM (View Pevaryl Cream Review and Pevaryl Cream Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

5611013-6 | Anaphylactic Shock
Adverse event was reported on Jan 25, 2008 by a Female patient taking Zinacef (View Usage) (Dosage: ) was diagnosed with antibiotic prophylaxis and. Location: GREECE , 49 years of age, Patient had the following side effects: anaphylactic shock.

5608003-6 | Erythema, Face Oedema, Hyperhidrosis, Hypoaesthesia, Lip Disorder, Oedema Peripheral, Pallor, Vomiting
on Jan 22, 2008 Female patient from POLAND , child 7 years of age, weighting 105.8 lb, was treated with Zinacef (View Usage). After Zinacef was administered, patient had the following side effects: erythema, face oedema, hyperhidrosis, hypoaesthesia, lip disorder, oedema peripheral, pallor, vomiting. Zinacef dosage: .

5607986-8 | Anaphylactic Shock
on Jan 25, 2008 Female patient from GREECE , 49 years of age, was diagnosed with antibiotic prophylaxis and was treated with Zinacef (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock. Zinacef dosage: .

5541787-4 | Anxiety, Chest Discomfort, Dyspnoea
Patient was taking Zinacef (View Usage). Patient had the following side effects: anxiety (What is anxiety?), chest discomfort, dyspnoea on Dec 06, 2007 from PAKISTAN Additional patient health information: Female patient , 45 years of age, weighting 158.7 lb, was diagnosed with multiple injuries and. Zinacef dosage: 1.5g Per Day. 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 Zinacef 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 Zinacef quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Zinacef 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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zinacef Episodes: 4: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: zoledronic Episodes: 1: Diagnosed with major depression.Side ...

CORNEAL OPACITY, view Drugs and Side Effects associated with CORNEAL OPACITY, ,CORNEAL OPACITY NEVANAC,CORNEAL OPACITY ZINACEF,CORNEAL OPACITY MIOCHOL,CORNEAL OPACITY ...

During the same period patient was treated with ZINACEF (View Zinacef Review and Zinacef Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ).

DIUREX (View Diurex Review and Diurex Label ), DIFORMIN (View Diformin Review and Diformin Label ), ZINACEF /UNK/ (View Zinacef /unk/ Review and Zinacef /unk/ Label ...

During the same period patient was treated with ZINACEF (0.75 G Qd) (View Zinacef Review and Zinacef Label ), NETILMICIN SULFATE (200 Mg Once Iv) (View Netilmicin Sulfate ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

The cephalosporin family includes cephalexin (Keflex), cefaclor (Ceclor), efuroxime (Zinacef), cefpodoxime (Vantin), cefprozil (Cefzil), and many injectable forms.

... Phenylephrine Label ), BENOXINATE HYDROCHLORIDE (View Benoxinate Hydrochloride Review and Benoxinate Hydrochloride Label ), ZINACEF (View Zinacef Review and Zinacef Label ).

The cephalosporin family includes cephalexin (Keflex), cefaclor (Ceclor), efuroxime (Zinacef), cefpodoxime (Vantin), cefprozil (Cefzil), and many injectable forms.

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Zinacef Reactions
Agranulocytosis
Anaphylactic Reaction
Anaphylactic Shock
Blood Pressure Decreased
Bronchospasm
Chills
Corneal Opacity
Cyanosis
Diarrhoea
Dysgeusia
Dyspnoea
Erythema
Heart Rate Decreased
Hyperhidrosis
Hypersensitivity
Hypotension
Loss Of Consciousness
Malaise
NauseaWhat is Nausea?
Off Label Use
Product Quality Issue
Pruritus
Pyrexia
RashWhat is Rash?
Rash Erythematous
Syncope
Tachycardia
Urticaria
Visual Disturbance
Vomiting
Zinacef 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 Zinacef 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!