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Claritin (Loratadine) - Adverse Event Reports - Hospitalization - Malaise

 



Index of reports > Cases resulting in hospitalization (19) > Cases with Malaise (4)

Below is the selection of adverse event reports related to Claritin (Loratadine) that includes cases resulting in hospitalization where reactions include malaise.

Adverse event in 59 year old male receiving Claritin (Loratadine)

Reported by a physician from Japan on 2007-06-11

Patient: 59 year old male, weighing 65.0 kg (143.0 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Jaundice, Hepatic Function Abnormal, Alanine Aminotransferase Increased, Chromaturia, Duodenal Obstruction, Malaise, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Claritin (Loratadine)



Adverse event in 59 year old male receiving Claritin (Loratadine)

Reported by a physician from Japan on 2007-04-30

Patient: 59 year old male, weighing 65.0 kg (143.0 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Jaundice, Malaise, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Chromaturia

Adverse event resulted in: hospitalization

Suspect drug(s):
Claritin (Loratadine)



Adverse event in 87 year old female receiving Claritin (Loratadine)

Reported by a health professional (non-physician/pharmacist) from France on 2007-03-14

Patient: 87 year old female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Malaise, Vertigo, Fall

Adverse event resulted in: hospitalization

Suspect drug(s):
Amlodipine
    Administration route: Oral

Xanax
    Administration route: Oral

Lasix
    Administration route: Oral

Esidrix
    Administration route: Oral

Stablon
    Administration route: Oral

Claritin
    Administration route: Oral

Vastarel
    Dosage: daily dose:70mg-freq:daily

Mopral
    Dosage: daily dose:20mg-freq:daily

Kardegic
    Dosage: daily dose:75mg-freq:daily

Diffu K
    Dosage: text:^6^-freq:daily



Adverse event in 87 year old female receiving Claritin (Loratadine)

Reported by a individual with unspecified qualification from France on 2007-03-12

Patient: 87 year old female, weighing 50.0 kg (110.0 pounds)

Adverse reactions / side effects: Malaise, Wound, Dizziness, Fall

Adverse event resulted in: hospitalization

Suspect drug(s):
Amlodipine
    Dosage: 5 mg, qd
    Administration route: Oral

Claritin
    Dosage: 10 mg, qd
    Administration route: Oral
    End date: 2007-01-15

Vastarel
    Dosage: 35 mg, bid
    Administration route: Oral
    End date: 2007-01-06

Esidrix
    Dosage: 25 mg, qd
    Administration route: Oral

Lasix
    Dosage: 20 mg/day
    Administration route: Oral

Xanax
    Dosage: 0.25 mg/day
    Administration route: Oral
    End date: 2007-01-17

Stablon
    Dosage: 12.5 mg, qd
    Administration route: Oral

Other drugs received by patient: Mopral; Kardegic

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