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Bone Side Effects Report #5649860-7
Consumer or non-health professional from UNITED STATES reported BONE problem on Jan 02, 2008. Female patient, 85 years of age, was diagnosed with bone disorder and was treated with BONE. After drug was administered, patient experienced the following problems/side effects: staphylococcal infection, walking aid user, . BONE dosage: unknown. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5490329-0
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Oct 05, 2007. Male patient, 32 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: mobility decreased, walking aid user, wheelchair user, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with AVONEX. Patient died on 09/01/2007.

Avonex Side Effects Report #5741862-5
Consumer or non-health professional from UNITED STATES reported AVONEX problem on May 05, 2008. Female patient, 70 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, walking aid user, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Levaquin Side Effects Report #5699230-0
LEVAQUIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 07, 2008. Male patient, 65 years of age, weighting 190.0 lb, was diagnosed with sinusitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: tendon injury, walking aid user, . LEVAQUIN dosage: unknown. Patient recovered.


Altace Side Effects Report #5702330-X
Consumer or non-health professional from UNITED STATES reported ALTACE problem on Apr 01, 2008. Female patient was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: asthenia, walking aid user, . ALTACE dosage: 2.5 MG, QD. During the same period patient was treated with DIURAL, CORTISONE. Patient recovered.

Bone Side Effects Report #5649839-5
BONE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 02, 2008. Female patient, 85 years of age, was diagnosed with bone disorder and was treated with BONE. After drug was administered, patient experienced the following problems/side effects: post procedural complication, staphylococcal infection, walking aid user, . BONE dosage: unknown. Patient was hospitalized. Patient recovered.

Vytorin Side Effects Report #5601189-9
Consumer or non-health professional from UNITED STATES reported VYTORIN problem on Jan 22, 2008. Female patient, weighting 150.0 lb, was diagnosed with blood cholesterol increased and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, myalgia, walking aid user, . VYTORIN dosage: unknown. Patient recovered.

Crestor Side Effects Report #5566030-1
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 18, 2007. Female patient, 75 years of age, was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: dysarthria, transient ischaemic attack, walking aid user, . CRESTOR dosage: unknown. Patient recovered.

Byetta Side Effects Report #5577194-8
Consumer or non-health professional from UNITED STATES reported BYETTA problem on July 26, 2007. Male patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: bedridden, blood glucose increased, walking aid user, . BYETTA dosage: unknown. Patient recovered.


Sotalol Side Effects Report #5399008-1
SOTALOL HYDROCHLORIDE problem was reported by a Health Professional from SWEDEN on July 23, 2007. Male patient, 46 years of age, was treated with SOTALOL HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis, thrombosis, walking aid user, . SOTALOL HYDROCHLORIDE dosage: unknown. During the same period patient was treated with WARFARIN, ATORVASTATIN CALCIUM. Patient recovered.

Sotalol Side Effects Report #5401093-5
Consumer or non-health professional from UNITED STATES reported SOTALOL HYDROCHLORIDE problem on July 25, 2007. Male patient, 46 years of age, was treated with SOTALOL HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis, thrombosis, walking aid user, . SOTALOL HYDROCHLORIDE dosage: unknown. During the same period patient was treated with WARFARIN, ATORVASTATIN CALCIUM. Patient recovered.

Sotalol Side Effects Report #5399008-1
SOTALOL HYDROCHLORIDE problem was reported by a Health Professional from SWEDEN on July 23, 2007. Male patient, 46 years of age, was treated with SOTALOL HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis, thrombosis, walking aid user, . SOTALOL HYDROCHLORIDE dosage: unknown. During the same period patient was treated with WARFARIN, ATORVASTATIN CALCIUM. Patient recovered.

Sotalol Side Effects Report #5401093-5
Consumer or non-health professional from UNITED STATES reported SOTALOL HYDROCHLORIDE problem on July 25, 2007. Male patient, 46 years of age, was treated with SOTALOL HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis, thrombosis, walking aid user, . SOTALOL HYDROCHLORIDE dosage: unknown. During the same period patient was treated with WARFARIN, ATORVASTATIN CALCIUM. Patient recovered.

Byetta Side Effects Report #5795170-7
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Female patient, 72 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose abnormal, malaise, walking aid user, . BYETTA dosage: unknown. Patient recovered.


Boniva Side Effects Report #5752814-3
Physician from UNITED STATES reported BONIVA problem on May 27, 2008. Female patient, 83 years of age, weighting 150.0 lb, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, bone pain, walking aid user, . BONIVA dosage: unknown. Patient recovered.