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Index of reports
> Cases resulting in a serious event (2)
Below is the selection of adverse event reports related to Levothroid (Levothyroxine) that includes cases resulting in a serious event.
Adverse event in 39 year old female receiving Levothroid (Levothyroxine)
Reported by a consumer/non-health professional from United States on 2007-07-25
Patient: 39 year old female
Adverse reactions / side effects: Blood Thyroid Stimulating Hormone Decreased, Hepatic Steatosis
Suspect drug(s):
Levothroid
Dosage: 112 mcg qd; po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2005-01-01
End date: 2007-07-01
Levothroid
Dosage: 110 mcg qd; po
Administration route: Oral
Indication: Hypothyroidism
End date: 2005-01-01
Levothroid
Dosage: 125 mcg qd;po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2007-07-02
Adverse event in 68 year old female receiving Levothroid (Levothyroxine)
Reported by a individual with unspecified qualification from United States on 2007-01-29
Patient: 68 year old female, weighing 81.6 kg (179.6 pounds)
Adverse reactions / side effects: Weight Increased, Fatigue, Alopecia, DRY Skin, Gastrooesophageal Reflux Disease
Suspect drug(s):
Levothroid
Dosage: 125 mcg qd po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-05-01
End date: 2006-07-01
Levothroid
Dosage: 125 mcg qd po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-08-01
Levothroid
Dosage: 125 mcg q07od po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-07-01
End date: 2006-08-01
Levothroid
Dosage: 62.5 mg qod po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2006-07-01
End date: 2006-08-01
Levothroid
Dosage: 150 mcg qd po
Administration route: Oral
Indication: Hypothyroidism
Start date: 2004-01-01
End date: 2006-05-01
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