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Augmentin (Amoxicillin / Clavulanate) - Pyrexia - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Pyrexia (13)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Augmentin (Amoxicillin / Clavulanate) where reactions include pyrexia. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Augmentin side effects in male

Reported by a physician from France on 2012-06-08

Patient: male

Reactions: Mucosal Inflammation, Pain in Extremity, Skin Lesion, Toxic Epidermal Necrolysis, General Physical Health Deterioration, Pyrexia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Bronchokod
    Indication: Bronchial Disorder
    Start date: 2012-03-07
    End date: 2012-03-13

Acetaminophen W / Codeine
    Indication: Sciatica
    Start date: 2012-02-07
    End date: 2012-02-14

Acetylcysteine
    Indication: Bronchial Disorder
    Start date: 2012-03-07
    End date: 2012-03-13

Augmentin
    Administration route: Oral
    Indication: Bronchial Disorder
    Start date: 2012-03-07
    End date: 2012-03-14

Temazepam
    Indication: Sciatica
    Start date: 2012-02-01
    End date: 2012-03-13

Voltaren
    Indication: Sciatica
    Start date: 2012-02-07
    End date: 2012-02-14

Prednisolone
    Indication: Sciatica
    Start date: 2012-02-01
    End date: 2012-03-13

Nexium
    Administration route: Oral
    Indication: Sciatica
    Start date: 2012-02-07
    End date: 2012-03-13

Other drugs received by patient: Medrol; Claritin; Chibrocadron



Possible Augmentin side effects in male

Reported by a health professional (non-physician/pharmacist) from France on 2012-06-08

Patient: male

Reactions: Agitation, Confusional State, Skin Exfoliation, Pain in Extremity, General Physical Health Deterioration, Toxic Epidermal Necrolysis, Pyrexia, Multi-Organ Failure, Skin Lesion, Conjunctival Hyperaemia, Acute Respiratory Distress Syndrome, Septic Shock, Oral Mucosa Erosion

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Prednisolone
    Indication: Pain
    Start date: 2012-02-01
    End date: 2012-03-13

Voltaren
    Indication: Back Pain
    Start date: 2012-02-07
    End date: 2012-02-14

Temazepam
    Indication: Pain
    Start date: 2012-02-01
    End date: 2012-03-13

Acetaminophen W / Codeine
    Indication: Back Pain
    Start date: 2012-02-07
    End date: 2012-02-14

Nexium
    Indication: Back Pain
    Start date: 2012-02-07
    End date: 2012-02-13

Augmentin
    Indication: Bronchial Disorder
    Start date: 2012-03-07
    End date: 2012-03-14

Acetylcysteine
    Indication: Bronchial Disorder
    Start date: 2012-03-07
    End date: 2012-03-13

Bronchokod
    Indication: Bronchial Disorder
    Start date: 2012-03-07
    End date: 2012-03-13



Possible Augmentin side effects in female

Reported by a physician from France on 2012-06-04

Patient: female

Reactions: Rash Scarlatiniform, Pyrexia, Eosinophilia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Tramadol HCL
    Administration route: Oral
    Indication: Pain
    Start date: 2011-09-03
    End date: 2012-01-31

Duphalac
    Administration route: Oral
    Indication: Constipation
    Start date: 2011-11-24
    End date: 2012-01-31

Augmentin
    Administration route: Oral
    Indication: Bronchitis
    Start date: 2012-01-25

Other drugs received by patient: Bisoprolol Fumarate; Vitamin D; Fluconazole; Pyostacine; Mianserin Hydrochloride; Rocephin; Solian; Potassium Chloride; Solian



Possible Augmentin side effects in male

Reported by a physician from United States on 2012-05-17

Patient: male, weighing 83.6 kg (183.9 pounds)

Reactions: Alcohol Abuse, Pancytopenia, Pyrexia, Transaminases Increased, Fall, Concomitant Disease Progression, Hepatic Steatosis, Hepatic Enzyme Increased, Renal Failure Acute

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Zortress
    Dosage: 1.5 mg, q12h
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2009-07-23
    End date: 2011-05-25

Augmentin
    Dosage: 500 mg, qd
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2010-09-29
    End date: 2010-10-06

Tacrolimus
    Dosage: 1 g, unk
    Indication: Liver Transplant
    Start date: 2009-06-22
    End date: 2011-06-26

Other drugs received by patient: Prograf



Possible Augmentin side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-14

Patient: male, weighing 83.6 kg (183.9 pounds)

Reactions: Alcohol Abuse, Pancytopenia, Pyrexia, Fall, Concomitant Disease Progression, Transaminases Increased, Hepatic Steatosis, Hepatic Enzyme Increased, Renal Failure Acute

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Tacrolimus
    Dosage: 1 g, unk
    Indication: Liver Transplant
    Start date: 2009-06-22
    End date: 2011-06-26

Zortress
    Dosage: 1.5 mg, q12h
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2009-07-23
    End date: 2011-05-25

Augmentin
    Dosage: 500 mg, qd
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2010-09-29
    End date: 2010-10-06

Other drugs received by patient: Prograf



Possible Augmentin side effects in male

Reported by a physician from Italy on 2012-05-10

Patient: male

Reactions: Rash, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Crestor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2012-04-26
    End date: 2012-04-27

Augmentin
    Dosage: 875/125 mg, 2 g daily
    Administration route: Oral
    Indication: Toothache
    Start date: 2012-04-26
    End date: 2012-04-27



Possible Augmentin side effects in 62 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-12-30

Patient: 62 year old female

Reactions: Gastrointestinal Haemorrhage, Acute Graft Versus Host Disease, Rash Papular, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms, Eosinophilia, Hepatitis Cholestatic, Renal Failure, Cardiac Failure

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Valaciclovir
    Dosage: 1 g / day
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-01-06
    End date: 2011-01-17

Augmentin
    Dosage: 1 g, tid
    Administration route: Oral
    Indication: Febrile Bone Marrow Aplasia
    Start date: 2011-01-29
    End date: 2011-02-04

Valaciclovir
    Dosage: 1 g / day
    Start date: 2011-02-08
    End date: 2011-02-17

Amlodipine Besylate
    Dosage: 10 mg / day
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-02-05
    End date: 2011-02-14

Augmentin
    Dosage: unk
    Start date: 2011-02-08
    End date: 2011-02-09

Levofloxacin
    Dosage: 1 g / day
    Administration route: Oral
    Indication: Lung Disorder
    Start date: 2011-02-07
    End date: 2011-02-15

Ceftriaxone
    Dosage: 1 g / day
    Indication: Lung Disorder
    Start date: 2011-02-09
    End date: 2011-02-12

Perindopril Erbumine
    Dosage: 20 mg / day
    Administration route: Oral
    Indication: Cardiac Failure
    Start date: 2011-02-06
    End date: 2011-02-17

Valaciclovir
    Dosage: 1 g / day
    Administration route: Oral
    Start date: 2011-02-01
    End date: 2011-02-04

Aldactone
    Dosage: 50 mg / day
    Administration route: Oral
    Indication: Cardiac Failure
    Start date: 2011-02-05
    End date: 2011-02-16

Other drugs received by patient: Fluconazole; Vancomycin; Lasix; Flagyl; Bisoprolol Fumarate; Valacyclovir Hydrochloride



Possible Augmentin side effects in 60 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-12-23

Patient: 60 year old female

Reactions: Renal Failure, Nausea, Cytolytic Hepatitis, Rash Morbilliform, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Acetaminophen and Tramadol HCL
    Dosage: 37.5/325 mg, 5 tablets daily
    Administration route: Oral
    Indication: Pain
    Start date: 2011-10-05
    End date: 2011-10-05

Augmentin
    Administration route: Oral
    Indication: Salivary Gland Calculus
    Start date: 2011-10-05
    End date: 2011-10-07

Other drugs received by patient: Amaryl



Possible Augmentin side effects in 62 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-12-22

Patient: 62 year old female

Reactions: Gastrointestinal Haemorrhage, Acute Graft Versus Host Disease, Rash Papular, Pyrexia, Drug Rash With Eosinophilia and Systemic Symptoms, Eosinophilia, Hepatitis Cholestatic, Multi-Organ Failure, Renal Failure, Cardiac Failure

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Aldactone
    Administration route: Oral
    Indication: Cardiac Failure
    Start date: 2011-02-05
    End date: 2011-02-16

Perindopril Erbumine
    Administration route: Oral
    Indication: Cardiac Failure
    Start date: 2011-02-06
    End date: 2011-02-17

Ceftriaxone
    Indication: Lung Disorder
    Start date: 2011-02-09
    End date: 2011-02-12

Valaciclovir
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-01-06
    End date: 2011-01-17

Valaciclovir
    Administration route: Oral
    Start date: 2011-02-08
    End date: 2011-02-17

Amlodipine Besylate
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-02-05
    End date: 2011-02-14

Valaciclovir
    Administration route: Oral
    Start date: 2011-02-01
    End date: 2011-02-04

Augmentin
    Start date: 2011-02-08
    End date: 2011-02-09

Levofloxacin
    Administration route: Oral
    Indication: Lung Disorder
    Start date: 2011-02-07
    End date: 2011-02-15

Augmentin
    Administration route: Oral
    Indication: Febrile Bone Marrow Aplasia
    Start date: 2011-01-29
    End date: 2011-02-04

Other drugs received by patient: Flagyl; Bisoprolol Fumarate; Clonazepam; Rituximab; Cytarabine; Ifosfamide; Etoposide; Ciproflaxacin; Piperacillin and Tazobactam; Fluconazole; Bicnu; Tobramycin; Imipenem / Cilastatin; Plerixafor; Vancomycin Hychloride; Lasix; Granocyte; Melphalan Hydrochloride



Possible Augmentin side effects in 60 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-11-16

Patient: 60 year old female

Reactions: Renal Failure, Nausea, Cytolytic Hepatitis, Rash Morbilliform, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Augmentin
    Administration route: Oral
    Indication: Salivary Gland Calculus
    Start date: 2011-10-05
    End date: 2011-10-07

Acetaminophen and Tramadol HCL
    Dosage: 37.5/325 mg, 5 tablets daily
    Administration route: Oral
    Indication: Pain
    Start date: 2011-10-05
    End date: 2011-10-05

Other drugs received by patient: Amaryl



Possible Augmentin side effects in 52 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2011-10-28

Patient: 52 year old female

Reactions: Lung Disorder, Hypersensitivity, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Myolastan
    Dosage: 50 mg
    Administration route: Oral
    Start date: 2011-08-20
    End date: 2011-08-30

Rovamycin
    Dosage: 1 500 000 ui
    Indication: Pneumonia
    Start date: 2011-08-25
    End date: 2011-08-26

Morphine Sulfate
    Dosage: 10 mg
    Administration route: Oral
    Start date: 2011-08-20
    End date: 2011-08-28

Primperan TAB
    Dosage: 10 mg
    Administration route: Oral
    Start date: 2011-08-21
    End date: 2011-08-28

Augmentin
    Dosage: 500/62.5 mg
    Indication: Pneumonia
    Start date: 2011-08-25
    End date: 2011-08-25

Acupan
    Dosage: unk
    Start date: 2011-08-19
    End date: 2011-08-30

Piperacillin and Tazobactam
    Dosage: 4 g
    Indication: Pneumonia
    Start date: 2011-08-25
    End date: 2011-08-30

Other drugs received by patient: Keppra; Potassium Chloride; Nicardipine HCL; Lovenox



Possible Augmentin side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2011-10-21

Patient: male, weighing 83.6 kg (183.9 pounds)

Reactions: Alcohol Abuse, Pancytopenia, Pyrexia, Concomitant Disease Progression, Fall, Transaminases Increased, Hepatic Steatosis, Hepatic Enzyme Increased, Renal Failure Acute

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Zortress
    Dosage: 1.5 mg, q12h
    Administration route: Oral
    Indication: Liver Transplant
    Start date: 2009-07-23
    End date: 2011-05-25

Tacrolimus
    Dosage: 1 g, unk
    Indication: Liver Transplant
    Start date: 2009-06-22
    End date: 2009-06-22

Augmentin
    Dosage: 500 mg, qd
    Administration route: Oral
    Indication: Sinusitis
    Start date: 2010-09-29
    End date: 2010-10-06

Other drugs received by patient: Prograf



Possible Augmentin side effects in 22 year old male

Reported by a health professional (non-physician/pharmacist) from United States on 2011-10-13

Patient: 22 year old male, weighing 57.1 kg (125.6 pounds)

Reactions: Respiratory Rate Increased, Viral Infection, Vomiting, Nausea, Chills, Urinary Tract Infection, Bone Pain, Pyrexia, Oropharyngeal Pain, Headache, Lower Respiratory Tract Infection, Haemoglobin Decreased, Skin Ulcer, Oxygen Saturation Decreased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
HQK-1001
    Dosage: 40 mg/kg, 1 d, oral
    Administration route: Oral
    Indication: Sickle Cell Anaemia
    Start date: 2011-07-11
    End date: 2011-09-15

Augmentin
    Dosage: 625 mg, 2 in 1 d, oral
    Administration route: Oral
    Indication: Sepsis
    Start date: 2011-09-05
    End date: 2011-09-15

Augmentin
    Dosage: 1.2 mg, intravenous
    Indication: Sepsis
    Start date: 2011-09-05
    End date: 2011-09-05

Voltaren
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-09-05

Ferrous Sulfate TAB
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-07-11

Other drugs received by patient: Folic Acid; Codeine Sulfate

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