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Side Efect (6)
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Common Magnex Side Effects

top 5 Magnex|Side efect|Deranged p|Lymphocyto|Yes adverse effects>>See All Magnex Side Effects

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Magnex adverse events reported to FDA.

Have You Experienced unusual Magnex symptoms? PatientsVille.com collects and analyzes Magnex side effect and adverse reports submitted by Magnex users, such as Echymosis on both upper limb and lower|.

Summary

FDA Adverse Reports: 21. View All

Magnex FDA safety alerts: No

Reported deaths: 9

Reported hospitalizations: 6

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1Side Efect
2Lymphocytosis
3Deranged Pt/inr
4Yes
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Echymosis on both upper limb and lower

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

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6930154-4 | Acute Respiratory Distress Syndrome, Atrial Fibrillation, Chest Discomfort, Decubitus Ulcer, Dyspnoea, Hyperhidrosis, Lower Respiratory Tract Infection, Pleural Effusion, Sepsis
on Aug 06, 2010 Male patient from INDIA , 69 years of age, was treated with Magnex (View Usage). Patient experienced the following unwanted or unexpected effects: acute respiratory distress syndrome, atrial fibrillation (What is atrial fibrillation?), chest discomfort, decubitus ulcer, dyspnoea, hyperhidrosis, lower respiratory tract infection, pleural effusion, sepsis (What is sepsis?). Magnex dosage: 1 G, 2x/day. Patient was hospitalized.

6924940-4 | Full Blood Count Decreased
Patient was taking Magnex (View Usage). Patient had the following side effects: full blood count decreased on Aug 05, 2010 from INDIA Additional patient health information: Female patient , 52 years of age, was diagnosed with sepsis (What is sepsis?) and. Magnex dosage: Unk.

6657412-5 | Thrombocytopenia
Adverse event was reported on Mar 18, 2010 by a Male patient taking Magnex (View Usage) (Dosage: 1 G, 2x/day) was diagnosed with surgery (What is surgery?) and. Location: INDIA , 45 years of age, After Magnex was administered, patient had the following side effects: thrombocytopenia.

6544858-9 | Pancytopenia
on Jan 13, 2010 Male patient from INDIA , 42 years of age, was diagnosed with head injury, epilepsy (What is epilepsy?) and was treated with Magnex (View Usage). Patient experienced the following unwanted or unexpected effects: pancytopenia. Magnex dosage: 2 G, 3x/day. During the same period patient was treated with PHENYTOIN (Unk) (View Phenytoin Review and Phenytoin Label ).


6398720-5 | Rash
on Oct 13, 2009 Female patient from INDIA , child 12 years of age, was diagnosed with wound infection and was treated with Magnex (View Usage). Patient had the following side effects: rash (What is rash?). Magnex dosage: 1.5 G, 2x/day. During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ).

6374439-1 | Cerebral Haemorrhage, Gastrointestinal Haemorrhage, Haematuria, Thrombocytopenia
Patient was taking Magnex (View Usage). After Magnex was administered, patient had the following side effects: cerebral haemorrhage, gastrointestinal haemorrhage, haematuria, thrombocytopenia on Sep 12, 2009 from INDIA Additional patient health information: Female patient , 28 years of age, was diagnosed with sepsis (What is sepsis?), multiple injuries and. Magnex dosage: 2 G, 2x/day. During the same period patient was treated with GENTAMICIN (View Gentamicin Review and Gentamicin Label ).

6348851-0 | Thrombocytopenia
Adverse event was reported on Sep 01, 2009 by a Female patient taking Magnex (View Usage) (Dosage: 2 G, 2x/day) was diagnosed with head injury and. Location: INDIA , 28 years of age, Patient experienced the following unwanted or unexpected effects: thrombocytopenia. During the same period patient was treated with GENTAMICIN (View Gentamicin Review and Gentamicin Label ).

6249362-3 | Rash
on Jun 16, 2009 Female patient from INDIA , child 12 years of age, was diagnosed with wound infection and was treated with Magnex (View Usage). Patient had the following side effects: rash (What is rash?). Magnex dosage: 1.5 G, 2x/day. During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ).

6228787-6 | Rash
on Jun 04, 2009 Female patient from INDIA , child 12 years of age, was diagnosed with wound infection and was treated with Magnex (View Usage). After Magnex was administered, patient had the following side effects: rash (What is rash?). Magnex dosage: 1.5 G, 2x/day. During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ).

5949046-2 | Blood Pressure Decreased, Pyrexia
Patient was taking Magnex (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, pyrexia on Oct 30, 2008 from INDIA Additional patient health information: Male patient , 28 years of age, was diagnosed with acute respiratory distress syndrome and. Magnex dosage: . Patient was hospitalized.

5774424-4 | Platelet Count Decreased, Septic Shock
Adverse event was reported on Jun 04, 2008 by a Male patient taking Magnex (View Usage) (Dosage: ) was diagnosed with peritonitis and. Location: INDIA , 23 years of age, weighting 165.3 lb, Patient had the following side effects: platelet count decreased, septic shock. During the same period patient was treated with METRONIDAZOLE (View Metronidazole Review and Metronidazole Label ), AMIKACIN (View Amikacin Review and Amikacin Label ), VITAMIN K TAB (View Vitamin K Tab Review and Vitamin K Tab Label ).

5751385-5 | Platelet Count Decreased
on May 19, 2008 Male patient from INDIA , 23 years of age, weighting 165.3 lb, was diagnosed with peritonitis and was treated with Magnex (View Usage). After Magnex was administered, patient had the following side effects: platelet count decreased. Magnex dosage: . During the same period patient was treated with METRONIDAZOLE HCL (View Metronidazole Hcl Review and Metronidazole Hcl Label ), AMIKACIN (View Amikacin Review and Amikacin Label ), VITAMIN K TAB (View Vitamin K Tab Review and Vitamin K Tab Label ).

5692206-9 | International Normalised Ratio Increased
on Mar 24, 2008 Male patient from INDIA , 50 years of age, was diagnosed with lung infection and was treated with Magnex (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Magnex dosage: . During the same period patient was treated with AMIKACIN (View Amikacin Review and Amikacin Label ). Patient was hospitalized.

5679593-2 | International Normalised Ratio Increased
Patient was taking Magnex (View Usage). Patient had the following side effects: international normalised ratio increased on Mar 13, 2008 from INDIA Additional patient health information: Male patient , 50 years of age, was diagnosed with lung infection and. Magnex dosage: . During the same period patient was treated with AMIKACIN (View Amikacin Review and Amikacin Label ). Patient was hospitalized.

5524689-9 | Septic Shock
Adverse event was reported on Nov 14, 2007 by a Male patient taking Magnex (View Usage) (Dosage: ) was diagnosed with sepsis (What is sepsis?) and. Location: INDIA , 30 years of age, weighting 176.4 lb, After Magnex was administered, patient had the following side effects: septic shock. During the same period patient was treated with MERONEM (View Meronem Review and Meronem Label ).

5517616-1 | Septic Shock
on Nov 02, 2007 Male patient from INDIA , 30 years of age, weighting 176.4 lb, was diagnosed with sepsis (What is sepsis?) and was treated with Magnex (View Usage). Patient experienced the following unwanted or unexpected effects: septic shock. Magnex dosage: . During the same period patient was treated with MERONEM (View Meronem Review and Meronem Label ).

5359577-4 | Graft Haemorrhage, Haematuria
on Jun 04, 2007 Female patient from INDIA , 80 years of age, was diagnosed with hydropneumothorax and was treated with Magnex (View Usage). Patient had the following side effects: graft haemorrhage, haematuria. Magnex dosage: . During the same period patient was treated with ENOXAPARIN SODIUM (Daily Dose:.4ml) (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), ACETYLSALICYLIC ACID/CLOPIDOGREL (Daily Dose:150mg) (View Acetylsalicylic Acid/clopidogrel Review and Acetylsalicylic Acid/clopidogrel Label ), I.V. SOLUTIONS (View I.v. Solutions Review and I.v. Solutions Label ).

5223110-8 | Disseminated Intravascular Coagulation, Haemorrhage Urinary Tract
Patient was taking Magnex (View Usage). After Magnex was administered, patient had the following side effects: disseminated intravascular coagulation, haemorrhage urinary tract on Jan 17, 2007 from INDIA Additional patient health information: Male patient , 60 years of age, was diagnosed with respiratory tract infection and. Magnex dosage: . During the same period patient was treated with AMIKACIN (View Amikacin Review and Amikacin Label ). Patient was hospitalized.

5223061-9 | Haemorrhage, Platelet Count Decreased
Adverse event was reported on Jan 17, 2007 by a Male patient taking Magnex (View Usage) (Dosage: ) was diagnosed with pneumonia aspiration and. Location: INDIA , 70 years of age, Patient experienced the following unwanted or unexpected effects: haemorrhage, platelet count decreased. During the same period patient was treated with AMIKACIN (View Amikacin Review and Amikacin Label ). Patient was hospitalized.

5205211-3 | Grand Mal Convulsion, Platelet Count Decreased, Renal Failure Acute, Respiratory Arrest
on Dec 30, 2006 Male patient from INDIA , 17 years of age, weighting 110.2 lb, was diagnosed with liver disorder and was treated with Magnex (View Usage). Patient had the following side effects: grand mal convulsion, platelet count decreased, renal failure acute, respiratory arrest. Magnex dosage: . During the same period patient was treated with DALACIN S (View Dalacin S Review and Dalacin S Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), VITAMIN K (View Vitamin K Review and Vitamin K Label ).

5195280-1 | Grand Mal Convulsion, Platelet Count Decreased, Renal Failure Acute, Respiratory Arrest
on Dec 01, 2006 Male patient from INDIA , 17 years of age, weighting 110.2 lb, was diagnosed with liver disorder and was treated with Magnex (View Usage). After Magnex was administered, patient had the following side effects: grand mal convulsion, platelet count decreased, renal failure acute, respiratory arrest. Magnex dosage: . During the same period patient was treated with DALACIN S (View Dalacin S Review and Dalacin S Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), VITAMIN K (View Vitamin K Review and Vitamin K Label ).


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Magnex 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 Magnex 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 Magnex quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Magnex 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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Magnex Reactions
Acute Respiratory Distress Syndrome
Atrial FibrillationWhat is Atrial fibrillation?
Blood Pressure Decreased
Cerebral Haemorrhage
Chest Discomfort
Death
Decubitus Ulcer
Disseminated Intravascular Coagulation
Dyspnoea
Full Blood Count Decreased
Gastrointestinal Haemorrhage
Graft Haemorrhage
Grand Mal Convulsion
Haematuria
Haemorrhage
Haemorrhage Urinary Tract
Hyperhidrosis
International Normalised Ratio Increased
Lower Respiratory Tract Infection
Pancytopenia
Platelet Count Decreased
Pleural Effusion
Pyrexia
RashWhat is Rash?
Renal Failure Acute
Respiratory Arrest
SepsisWhat is Sepsis?
Septic Shock
Thrombocytopenia
Magnex 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 Magnex 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!