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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Maxipime (Cefepime). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (46)
Cases resulting in a serious event (41)
Cases resulting in death (13)
Cases resulting in life threatening events (6)
Cases resulting in hospitalization (21)
Cases resulting in disability (1)
Cases resulting in other serious reactions (7)
Below is a sample of reports where side effects / adverse reactions may be related to Maxipime (Cefepime). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in female receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-10-26
Patient: female, weighing 47.0 kg (103.4 pounds)
Adverse reactions / side effects: Interstitial Lung Disease, Febrile Neutropenia, Neutrophil Count Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Farmorubicin RD
Dosage: daily dose:120mg-freq:every days
Indication: Breast Cancer
Farmorubicin RD
Dosage: daily dose:90-freq:every days
Endoxan
Dosage: daily dose:900mg-freq:every days
Indication: Breast Cancer
Endoxan
Dosage: daily dose:700mg-freq:every days
Gran
Dosage: daily dose:75mcg-freq:every days
Maxipime
Dosage: daily dose:2000mg
Start date: 2007-09-17
End date: 2007-09-19
Adverse event in 58 year old male receiving Maxipime (Cefepime)
Reported by a individual with unspecified qualification from Japan on 2007-10-19
Patient: 58 year old male
Adverse reactions / side effects: Jaundice, Gastrointestinal Haemorrhage, Leukaemia Recurrent, Hypokalaemia, Haematemesis, Disease Progression, Liver Disorder, Blood Uric Acid Decreased, Blood Lactate Dehydrogenase Increased, Acute Myeloid Leukaemia, Anaemia, Haematuria, Febrile Neutropenia, Condition Aggravated, Hypoproteinaemia, Platelet Count Decreased, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Novantrone
Dosage: see image
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-03-29
End date: 2007-03-30
Novantrone
Dosage: see image
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-03-30
End date: 2007-03-30
Novantrone
Dosage: see image
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-04-13
End date: 2007-04-13
Novantrone
Dosage: see image
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-04-25
End date: 2007-04-25
Mylotarg
Dosage: see image
Start date: 2007-03-02
End date: 2007-03-02
Mylotarg
Dosage: see image
Start date: 2007-03-16
End date: 2007-03-16
Itraconazole
Dosage: 200 mg, 1 in 1 days, intravenous (not otherwise specified)
Start date: 2007-03-23
End date: 2007-04-05
Maxipime
Dosage: see image
Start date: 2007-03-07
End date: 2007-03-12
Maxipime
Dosage: see image
Start date: 2007-03-18
End date: 2007-03-31
Other drugs received by patient: Idarubicin HCL
Adverse event in male receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-10-10
Patient: male, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Jaundice, Gastrointestinal Haemorrhage, Malignant Neoplasm Progression, Liver Disorder, Hypokalaemia, Haematemesis, Blood Uric Acid Decreased, C-Reactive Protein Increased, Blood Lactate Dehydrogenase Increased, Acute Myeloid Leukaemia, Anaemia, Haematuria, Febrile Neutropenia, Condition Aggravated, Hypoproteinaemia, Platelet Count Decreased, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Mylotarg
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-03-02
End date: 2007-03-02
Mylotarg
Start date: 2007-03-16
End date: 2007-03-16
Itrizole
Start date: 2007-03-23
End date: 2007-04-05
Maxipime
Start date: 2007-03-07
End date: 2007-03-12
Maxipime
Start date: 2007-03-18
End date: 2007-03-31
Novantrone
Dosage: unknown
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-03-29
End date: 2007-03-30
Novantrone
Dosage: unknown
Start date: 2007-03-30
End date: 2007-03-30
Novantrone
Dosage: unknown
Start date: 2007-04-13
End date: 2007-04-13
Novantrone
Dosage: unknown
Start date: 2007-04-25
End date: 2007-04-25
Other drugs received by patient: Idamycin
Adverse event in 65 year old female receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-03
Patient: 65 year old female
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: life threatening event
Suspect drug(s):
Maxipime
Indication: Febrile Neutropenia
Endoxan
Epirubicin
Gran
Adverse event in 65 year old female receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-10-02
Patient: 65 year old female
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: hospitalization
Suspect drug(s):
Farmorubicin RD
Indication: Breast Cancer
Endoxan
Indication: Breast Cancer
Gran
Maxipime
Adverse event in 64 year old female receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-31
Patient: 64 year old female
Adverse reactions / side effects: C-Reactive Protein Increased, Pancytopenia, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tagamet
Start date: 2007-06-13
End date: 2007-06-22
Omeprazole
Start date: 2007-05-22
End date: 2007-06-12
Ciprofloxacin
Start date: 2007-06-12
End date: 2007-06-15
Prodif
Start date: 2007-06-13
End date: 2007-06-18
Vancomycin Hydrochloride
Start date: 2007-06-13
End date: 2007-06-14
Maxipime
Start date: 2007-06-15
End date: 2007-06-18
Other drugs received by patient: Gran; Predonine
Adverse event in 64 year old female receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-07-30
Patient: 64 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Agranulocytosis, C-Reactive Protein Increased, Small Intestine Carcinoma, Hyponatraemia, Pancytopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Zantac 150
Dosage: 150mg per day
Indication: Gastric Ulcer Haemorrhage
Start date: 2007-06-13
End date: 2007-06-28
Maxipime
Dosage: 1g twice per day
Indication: Sepsis
Start date: 2007-06-15
End date: 2007-06-18
Prodif
Dosage: 400mg per day
Indication: Sepsis
Start date: 2007-06-13
End date: 2007-06-18
Vancomycin
Indication: Sepsis
Start date: 2007-06-13
End date: 2007-06-14
Other drugs received by patient: Omeprazole; Ciprofloxacin; Predonine; Tagamet; Hydrocortone; Predonine; Gran
Adverse event in 64 year old female receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-07-27
Patient: 64 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Agranulocytosis, C-Reactive Protein Increased, Small Intestine Carcinoma, Pancytopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Zantac 150
Dosage: 150mg per day
Indication: Gastric Ulcer Haemorrhage
Start date: 2007-06-13
End date: 2007-06-28
Maxipime
Dosage: 1g twice per day
Indication: Sepsis
Start date: 2007-06-15
End date: 2007-06-18
Prodif
Dosage: 400mg per day
Indication: Sepsis
Start date: 2007-06-13
End date: 2007-06-18
Vancomycin
Indication: Sepsis
Start date: 2007-06-13
End date: 2007-06-14
Other drugs received by patient: Omeprazole; Ciprofloxacin; Predonine; Tagamet; Hydrocortone; Predonine; Gran
Adverse event in male receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-26
Patient: male
Adverse reactions / side effects: Thrombocytopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Maxipime (Cefepime)
Adverse event in 80 year old male receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-26
Patient: 80 year old male
Adverse reactions / side effects: Confusional State
Suspect drug(s):
Maxipime (Cefepime)
Other drugs received by patient: Vancomycin; Coreg; Ranitidine
Adverse event in receiving Maxipime (Cefepime)
Reported by a consumer/non-health professional from United States on 2007-07-26
Patient:
Adverse reactions / side effects: Neutropenia, White Blood Cell Count Increased
Suspect drug(s):
Maxipime (Cefepime)
Adverse event in 48 year old male receiving Maxipime (Cefepime)
Reported by a consumer/non-health professional from Singapore on 2007-07-25
Patient: 48 year old male
Adverse reactions / side effects: Drug Ineffective, Sepsis
Adverse event resulted in: death
Suspect drug(s):
Maxipime (Cefepime)
Other drugs received by patient: Meronem; Ciproxin
Adverse event in female receiving Maxipime (Cefepime)
Reported by a physician from Mexico on 2007-07-13
Patient: female
Adverse reactions / side effects: Drug Ineffective, Cardiac Arrest
Adverse event resulted in: death
Suspect drug(s):
Maxipime (Cefepime)
Other drugs received by patient: Platelets; Plasma; Vitamin K
Adverse event in 52 year old female receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-10
Patient: 52 year old female, weighing 43.7 kg (96.1 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal
Suspect drug(s):
Meropenem
Indication: Neutrophil Count Decreased
Start date: 2007-04-15
End date: 2007-04-16
Zovirax
Administration route: Oral
Indication: Herpes Zoster
Start date: 2007-04-05
End date: 2007-04-16
Neutrogin
Indication: Stem Cell Transplant
Start date: 2007-04-07
End date: 2007-04-16
Maxipime
Indication: Neutrophil Count Decreased
Start date: 2007-04-08
End date: 2007-04-15
Exacin Injection 400
Indication: Neutrophil Count Decreased
Start date: 2007-04-08
End date: 2007-04-15
Targocid
Indication: Neutrophil Count Decreased
Start date: 2007-04-15
End date: 2007-04-16
Other drugs received by patient: Bonalon Tablet; Estriel; Diflucan; Mucosta; Takepron; Pantosin; Magnesium Oxide; Depas; Fulcaliq No.1; Platelets; Platelets; RBC Concentrate Transfusion
Adverse event in 64 year old male receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-06-28
Patient: 64 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, White Blood Cell Count Decreased, Blood Urea Increased, Alanine Aminotransferase Increased, Blood Potassium Increased, Condition Aggravated, Convulsion, Liver Disorder, Leukaemia, Multi-Organ Failure, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Creatinine Increased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Ambisome
Dosage: 150 mg, uid/qd, iv drip
Indication: Fungal Infection
Start date: 2007-05-03
End date: 2007-05-15
Ciproflaxacin
Dosage: 600 mg, uid/qd, iv drip
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-27
End date: 2007-05-08
Targocid
Dosage: 400 mg, uid/qd, iv drip
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-27
End date: 2007-05-10
Potassium Chloride
Dosage: see image
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-02
End date: 2007-05-02
Potassium Chloride
Dosage: see image
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-03
End date: 2007-05-05
Potassium Chloride
Dosage: see image
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-06
End date: 2007-05-13
Maxipime
Dosage: 4 g, uid/qd, iv nos
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-09
End date: 2007-05-15
Zyvox
Dosage: uid/qd, iv drip
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-11
End date: 2007-05-15
Other drugs received by patient: Vfend; Platelets; RED Blood Cells; Neutrogin (Lenograstim); Physio (Glucose, Sodium Acetate, Calcium Gluconate, Sodium Chloride, P; Fulcaliq; Rituxan
Adverse event in 95 year old female receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-06-22
Patient: 95 year old female
Adverse reactions / side effects: Depressed Level of Consciousness, Strabismus, Convulsion
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Maxipime (Cefepime)
Adverse event in 64 year old male receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-06-20
Patient: 64 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, White Blood Cell Count Decreased, Blood Urea Increased, Alanine Aminotransferase Increased, Blood Potassium Increased, Condition Aggravated, Convulsion, Liver Disorder, Leukaemia, Multi-Organ Failure, Aspartate Aminotransferase Increased, Lung Cancer Metastatic, Platelet Count Decreased, Blood Creatinine Increased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Ambisome
Dosage: 150 mg, uid/qd, iv drip
Indication: Fungal Infection
Start date: 2007-05-03
End date: 2007-05-15
Ciprofloxacin HCL
Dosage: 600 mg, uid/qd, iv drip
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-27
End date: 2007-05-08
Targocid
Dosage: 400 mg, uid/qd, iv drip
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-27
End date: 2007-05-10
Potassium Chloride
Dosage: see image
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-02
End date: 2007-05-02
Potassium Chloride
Dosage: see image
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-03
End date: 2007-05-05
Potassium Chloride
Dosage: see image
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-06
End date: 2007-05-13
Maxipime
Dosage: 4 g, uid/qd, iv nos
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-09
End date: 2007-05-15
Zyvox
Dosage: uid/qd, iv drip
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-11
End date: 2007-05-15
Other drugs received by patient: Vfend; Platelets; RED Blood Cells; Neutrogin (Lenograstim); Physio (Glucose, Sodium Acetate, Calcium Gluconate, Sodium Chloride,; Fulcaliq; Rituxan
Adverse event in male receiving Maxipime (Cefepime)
Reported by a physician from Japan on 2007-05-15
Patient: male, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Blast Cell Count Increased, Haematuria, Anaemia, Blood Lactate Dehydrogenase Increased, Condition Aggravated, Hypokalaemia, C-Reactive Protein Increased, Platelet Count Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Mylotarg
Indication: Acute Myeloid Leukaemia Recurrent
Start date: 2007-03-02
End date: 2007-03-02
Mylotarg
Start date: 2007-03-16
End date: 2007-03-16
Itraconazole
Start date: 2007-03-23
End date: 2007-04-05
Maxipime
Start date: 2007-03-07
End date: 2007-03-12
Maxipime
Start date: 2007-03-18
End date: 2007-03-31
Other drugs received by patient: Idamycin; Novantrone
Adverse event in 77 year old female receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-05-14
Patient: 77 year old female
Adverse reactions / side effects: Ventricular Tachycardia, Convulsion
Adverse event resulted in: life threatening event
Suspect drug(s):
Maxipime (Cefepime)
Other drugs received by patient: Sigmart; Hustazol; Gramalil; Takepron; Aspirin; Hirnamin; Frandol Tape S; Procylin
Adverse event in 34 year old female receiving Maxipime (Cefepime)
Reported by a pharmacist from United States on 2007-05-08
Patient: 34 year old female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Burning Sensation, Rash, Infusion Related Reaction
Suspect drug(s):
Maxipime (Cefepime)
Adverse event in 83 year old female receiving Maxipime (Cefepime)
Reported by a physician from Austria on 2007-05-04
Patient: 83 year old female
Adverse reactions / side effects: Cardiac Failure
Adverse event resulted in: death
Suspect drug(s):
Maxipime (Cefepime)
Adverse event in 65 year old male receiving Maxipime (Cefepime)
Reported by a physician from Austria on 2007-05-04
Patient: 65 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Maxipime
Indication: Respiratory Tract Infection
Start date: 2001-12-21
End date: 2001-12-24
Maxipime
Indication: Wound
Start date: 2001-12-21
End date: 2001-12-24
Maxipime
Indication: Sepsis
Start date: 2001-12-21
End date: 2001-12-24
Ciprofloxacin Hydrochloride
Indication: Respiratory Tract Infection
Start date: 2001-12-21
End date: 2001-12-24
Ciprofloxacin Hydrochloride
Indication: Sepsis
Start date: 2001-12-21
End date: 2001-12-24
Ciprofloxacin Hydrochloride
Indication: Wound
Start date: 2001-12-21
End date: 2001-12-24
Adverse event in 77 year old female receiving Maxipime (Cefepime)
Reported by a physician from Austria on 2007-05-04
Patient: 77 year old female, weighing 120.0 kg (264.0 pounds)
Adverse reactions / side effects: Multi-Organ Failure
Adverse event resulted in: death
Suspect drug(s):
Maxipime
Indication: Lung Infection
Start date: 2004-01-17
End date: 2004-01-22
Maxipime
Indication: Genitourinary Tract Infection
Start date: 2004-01-17
End date: 2004-01-22
Gentamicin
Indication: Lung Infection
Start date: 2004-01-17
End date: 2004-01-22
Gentamicin
Indication: Genitourinary Tract Infection
Start date: 2004-01-17
End date: 2004-01-22
Adverse event in 82 year old female receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from Austria on 2007-05-04
Patient: 82 year old female, weighing 115.0 kg (253.0 pounds)
Adverse reactions / side effects: Multimorbidity
Adverse event resulted in: death
Suspect drug(s):
Maxipime
Indication: Respiratory Tract Infection
Start date: 2004-04-10
End date: 2004-04-20
Maxipime
Indication: Abdominal Infection
Start date: 2004-04-10
End date: 2004-04-20
Zyvox
Indication: Abdominal Infection
Start date: 2004-04-10
End date: 2004-04-20
Zyvox
Indication: Respiratory Tract Infection
Start date: 2004-04-10
End date: 2004-04-20
Adverse event in male receiving Maxipime (Cefepime)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-30
Patient: male, weighing 192.8 kg (424.1 pounds)
Adverse reactions / side effects: Rash Generalised
Suspect drug(s):
Maxipime
Dosage: 1gm every 12 hours picc line
Indication: Cellulitis
Start date: 2007-04-21
End date: 2007-04-24
Vancomycin
Dosage: 1500mg every 12 hours picc line
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