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ROTATOR CUFF SYNDROME side effect

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Botox Side Effects Report #5649174-5
Health Professional from UNITED STATES reported BOTOX problem on Feb 25, 2008. Male patient was diagnosed with urinary tract disorder, benign prostatic hyperplasia and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . BOTOX dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5654448-8
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Male patient, 47 years of age, weighting 155.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . REBIF dosage: unknown. During the same period patient was treated with ADVIL LIQUID GELS. Patient recovered.

Avonex Side Effects Report #5664044-4
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Feb 28, 2008. Female patient, 48 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5667084-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Female patient, weighting 140.1 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . HUMIRA dosage: unknown. During the same period patient was treated with AZATHIOPRINE. Patient recovered.


Avonex Side Effects Report #5679639-1
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 11, 2008. Male patient, 57 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Avastin Side Effects Report #5616060-6
AVASTIN problem was reported by a Physician from UNITED STATES on Jan 29, 2008. Female patient was diagnosed with lung cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . AVASTIN dosage: 810 MG, Q3W. During the same period patient was treated with CARBOPLATIN, TAXOL, ARIMIDEX, TAXOTERE. Patient recovered.

Levaquin Side Effects Report #5642469-0
Physician from UNITED STATES reported LEVAQUIN problem on Feb 21, 2008. Male patient, weighting 150.0 lb, was diagnosed with postoperative wound infection and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, tendon rupture, . LEVAQUIN dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized and became disabled. Patient recovered.

Forteo Side Effects Report #5532285-2
FORTEO problem was reported by a Physician from UNITED STATES on Nov 21, 2007. Female patient, 60 years of age, weighting 176.0 lb, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . FORTEO dosage: unknown. During the same period patient was treated with ASPIRIN, CALCIUM, NEXIUM, CENTRUM SILVER, ZOCOR, VICODIN, PERCOCET, IBUPROFEN. Patient recovered.

Remicade Side Effects Report #5549796-6
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Dec 04, 2007. Female patient, weighting 162.0 lb, was diagnosed with arthritis, crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . REMICADE dosage: unknown. During the same period patient was treated with STEROIDS, BENADRYL. Patient recovered.


Levaquin Side Effects Report #5526531-9
LEVAQUIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2007. Female patient, 59 years of age, weighting 240.0 lb, was diagnosed with diverticulitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . LEVAQUIN dosage: unknown. Patient recovered.

Levaquin Side Effects Report #5538291-6
Physician from UNITED STATES reported LEVAQUIN problem on Aug 02, 2007. Female patient, 59 years of age, weighting 242.0 lb, was diagnosed with diverticulitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, tendon rupture, . LEVAQUIN dosage: 500 MG,. During the same period patient was treated with METRONIDAZOLE, LERTAB, DIOVAN, CO DIOVAN. Patient recovered.

Byetta Side Effects Report #5577529-6
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 25, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . BYETTA dosage: unknown. Patient recovered.

Humira Side Effects Report #5492555-3
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Oct 12, 2007. Female patient, weighting 185.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . HUMIRA dosage: unknown. During the same period patient was treated with SULFASALAZINE, METHOTREXATE, PREDNISOLONE, BETAMETHASONE, FOLIC ACID, INDAPAMIDE, IRBESARTAN. Patient was hospitalized and became disabled. Patient recovered.

Forteo Side Effects Report #5455306-4
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Female patient was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . FORTEO dosage: unknown. During the same period patient was treated with ASPIRIN, CALCIUM, NEXIUM, CENTRUM SILVER, ZOCOR, VICODIN, PERCOCET, IBUPROFEN. Patient recovered.


Humira Side Effects Report #5405588-X
Physician from UNITED STATES reported HUMIRA problem on July 26, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Ambien Side Effects Report #5385200-9
AMBIEN problem was reported by a Physician from UNITED STATES on July 06, 2007. Female patient, weighting 159.0 lb, was diagnosed with insomnia and was treated with AMBIEN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . AMBIEN dosage: 5 MG -BROKE IN HALF- ONE TIME DOSE PO. Patient recovered.

Ambien Side Effects Report #5385200-9
Physician from UNITED STATES reported AMBIEN problem on July 06, 2007. Female patient, weighting 159.0 lb, was diagnosed with insomnia and was treated with AMBIEN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . AMBIEN dosage: 5 MG -BROKE IN HALF- ONE TIME DOSE PO. Patient recovered.

Levaquin Side Effects Report #5701784-2
LEVAQUIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 10, 2008. Male patient, weighting 155.0 lb, was diagnosed with urinary tract infection and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . LEVAQUIN dosage: 500MG 1 X DAILY ORAL. Patient recovered.

Remicade Side Effects Report #5704281-3
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Apr 03, 2008. Female patient, weighting 162.0 lb, was diagnosed with arthritis, crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . REMICADE dosage: unknown. During the same period patient was treated with STEROIDS, BENADRYL. Patient recovered.


Rebif Side Effects Report #5323077-8
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2007. Female patient, 61 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . REBIF dosage: unknown. During the same period patient was treated with ADVIL. Patient was hospitalized. Patient recovered.

Crestor Side Effects Report #5236882-3
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Feb 24, 2005. Female patient, 65 years of age, weighting 175.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . CRESTOR dosage: 10 MG PO. During the same period patient was treated with BEXTRA. Patient recovered.

Levaquin Side Effects Report #5258441-9
LEVAQUIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 14, 2006. Female patient, 64 years of age, weighting 160.0 lb, was diagnosed with sinusitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . LEVAQUIN dosage: 750 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with RESTORIL, SYNTHROID, SINGULAR, CARDIZEM, NEXIUM, ASPIRIN. Patient recovered.

Levaquin Side Effects Report #5264942-X
Physician from UNITED STATES reported LEVAQUIN problem on Oct 03, 2005. Female patient, 51 years of age, weighting 180.0 lb, was diagnosed with postoperative wound infection and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . LEVAQUIN dosage: 500 MG, 2 IN 1 DAY, ORAL. During the same period patient was treated with PREVACID, ZOLOFT, ESTRACE, ACYCLOVIR, CRESTOR, DOXAPIN, SINGULAIR, OXYCONTIN. Patient was hospitalized. Patient recovered.

Levaquin Side Effects Report #5268165-X
LEVAQUIN problem was reported by a Health Professional from UNITED STATES on Mar 16, 2007. Female patient, 55 years of age, weighting 148.0 lb, was diagnosed with otitis media and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: rotator cuff syndrome, . LEVAQUIN dosage: 1 500 MG TABLET DAILY PO. Patient recovered.

Crestor Side Effects Report #5648818-1
Physician from JAPAN reported CRESTOR problem on Feb 28, 2008. Male patient, 72 years of age, weighting 134.5 lb, was diagnosed with hyperlipidaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: liver disorder, rotator cuff syndrome, . CRESTOR dosage: unknown. During the same period patient was treated with ANAESTHESIA, ASPIRIN, FRANDOL S, SIGMART, NORVASC, KERLONG, GLYBURIDE, BASEN OD. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5616310-6
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 23, 2008. Female patient, 59 years of age, weighting 145.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: exostosis, rotator cuff syndrome, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Crestor Side Effects Report #5632014-8
Physician from JAPAN reported CRESTOR problem on Feb 18, 2008. Male patient, 72 years of age, weighting 134.5 lb, was diagnosed with hyperlipidaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: liver disorder, rotator cuff syndrome, . CRESTOR dosage: unknown. During the same period patient was treated with ANAESTHESIA, ASPIRIN, FRANDOL S, SIGMART, NORVASC, KERLONG, GLYBURIDE, BASEN OD. Patient was hospitalized. Patient recovered.

Crestor Side Effects Report #5639033-6
CRESTOR problem was reported by a Physician from JAPAN on Feb 18, 2008. Male patient, 72 years of age, weighting 134.5 lb, was diagnosed with hyperlipidaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: liver disorder, rotator cuff syndrome, . CRESTOR dosage: unknown. During the same period patient was treated with ANAESTHESIA, ASPIRIN, FRANDOL S, SIGMART, NORVASC, KERLONG, GLYBURIDE, BASEN OD. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5640771-X
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 18, 2008. Male patient, weighting 205.0 lb, was diagnosed with pain, depression, breakthrough pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: inadequate analgesia, rotator cuff syndrome, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with REMERON, AVAPRO, LASIX, LISINOPRIL, TOPROL, OXYCODONE. Patient recovered.

Levaquin Side Effects Report #5607750-X
LEVAQUIN problem was reported by a Pharmacist from UNITED STATES on Jan 23, 2008. Female patient, weighting 168.0 lb, was diagnosed with sinusitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: exostosis, rotator cuff syndrome, tendonitis, . LEVAQUIN dosage: unknown. During the same period patient was treated with CYMBALTA, VOLTAREN. Patient recovered.

Levaquin Side Effects Report #5542993-5
Physician from UNITED STATES reported LEVAQUIN problem on July 25, 2007. Female patient, 63 years of age, weighting 169.0 lb, was diagnosed with sinusitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: musculoskeletal pain, rotator cuff syndrome, . LEVAQUIN dosage: 750 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with TOPROL, FUROSEMIDE, GLIPIZIDE ER, VYTORIN, ENALAPRIL MALEATE, AVANDIA, ZYRTEC. Patient recovered.

Forteo Side Effects Report #5446282-9
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 27, 2007. Female patient, 76 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: malaise, rotator cuff syndrome, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Seroquel Side Effects Report #5456720-3
Health Professional from UNITED STATES reported SEROQUEL problem on Feb 28, 2007. Male patient, 37 years of age, weighting 220.5 lb, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: arthropathy, rotator cuff syndrome, type 2 diabetes mellitus, . SEROQUEL dosage: unknown. During the same period patient was treated with PROZAC. Patient recovered.

Lipitor Side Effects Report #5423019-0
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Male patient, weighting 210.4 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: musculoskeletal disorder, rotator cuff syndrome, . LIPITOR dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5391599-X
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on July 09, 2007. Male patient, weighting 210.4 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: musculoskeletal disorder, rotator cuff syndrome, . LIPITOR dosage: unknown. Patient recovered.

Byetta Side Effects Report #5445269-X
BYETTA problem was reported by a Health Professional from UNITED STATES on May 29, 2007. Female patient, 47 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, rotator cuff syndrome, . BYETTA dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5391599-X
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on July 09, 2007. Male patient, weighting 210.4 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: musculoskeletal disorder, rotator cuff syndrome, . LIPITOR dosage: unknown. Patient recovered.

Byetta Side Effects Report #5445269-X
BYETTA problem was reported by a Health Professional from UNITED STATES on May 29, 2007. Female patient, 47 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, rotator cuff syndrome, . BYETTA dosage: unknown. Patient recovered.

Benicar Side Effects Report #5760623-4
Consumer or non-health professional from UNITED STATES reported BENICAR HCT problem on May 21, 2008. Female patient, 58 years of age, weighting 270.0 lb, was diagnosed with hypertension and was treated with BENICAR HCT. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, rotator cuff syndrome, . BENICAR HCT dosage: 40/12.5 MG (QD), PER ORAL; ABOUT ONE AND A HALF YEARS AGO. During the same period patient was treated with LYRICA, GAS ANESTHESIA. Patient recovered.

Humira Side Effects Report #5768451-0
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on June 02, 2008. Female patient, weighting 167.6 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: musculoskeletal pain, rotator cuff syndrome, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5771070-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on May 23, 2008. Male patient, weighting 202.2 lb, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site haemorrhage, rotator cuff syndrome, . HUMIRA dosage: unknown. Patient recovered.

Rebif Side Effects Report #5796682-2
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on June 17, 2008. Female patient, 66 years of age, weighting 205.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: no therapeutic response, rotator cuff syndrome, . REBIF dosage: unknown. Patient recovered.

Aspirin Side Effects Report #5728892-4
Consumer or non-health professional from UNITED STATES reported ASPIRIN problem on Apr 28, 2008. Male patient, 71 years of age, weighting 235.9 lb, was diagnosed with ischaemic heart disease prophylaxis and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: contusion, rotator cuff syndrome, . ASPIRIN dosage: TOTAL DAILY DOSE: 81 MG UNIT DOSE: 81 MG. During the same period patient was treated with OMEPRAZOLE, ALLOPURINOL, METOPROLOL TARTRATE, SIMVASTATIN. Patient recovered.

Risedronate Side Effects Report #5714331-6
RISEDRONATE problem was reported by a Pharmacist from SPAIN on Apr 08, 2008. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with RISEDRONATE. After drug was administered, patient experienced the following problems/side effects: articular calcification, rotator cuff syndrome, . RISEDRONATE dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with ENANTYUM. Patient recovered.

Humira Side Effects Report #5366029-4
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on June 12, 2007. Male patient, weighting 183.2 lb, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: fall, rotator cuff syndrome, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.

Byetta Side Effects Report #5319367-5
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on May 01, 2007. Female patient, 59 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, rotator cuff syndrome, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOVANCE. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5310790-1
Physician from UNITED STATES reported LIPITOR problem on Apr 17, 2007. Male patient, weighting 190.5 lb, was diagnosed with blood cholesterol increased, hyperlipidaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: musculoskeletal disorder, rotator cuff syndrome, . LIPITOR dosage: unknown. During the same period patient was treated with WELLBUTRIN, MAXZIDE, NORVASC. Patient recovered.

Lipitor Side Effects Report #5270397-1
LIPITOR problem was reported by a Physician from UNITED STATES on Mar 09, 2007. Male patient, weighting 195.1 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: musculoskeletal disorder, rotator cuff syndrome, . LIPITOR dosage: unknown. During the same period patient was treated with WELLBUTRIN, MAXZIDE, NORVASC. Patient recovered.

Humira Side Effects Report #5668467-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 22, 2008. Female patient, weighting 115.1 lb, was diagnosed with rheumatoid arthritis, gastric disorder, hypothyroidism, eye disorder, atrial fibrillation, cardiac disorder, blood pressure and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: accidental exposure, musculoskeletal pain, rotator cuff syndrome, . HUMIRA dosage: unknown. During the same period patient was treated with ESOMEPRAZOLE MAGNESIUM, SYNTHROID, PREDNISONE, PRESEVISION, MESALAMINE, WARFARIN, DIGITEC, LOSARTAN POTASSIUM. Patient recovered.

Namenda Side Effects Report #5685146-2
NAMENDA problem was reported by a Physician from UNITED STATES on Mar 14, 2008. Female patient, 85 years of age, was diagnosed with dementia and was treated with NAMENDA. After drug was administered, patient experienced the following problems/side effects: hyperproteinaemia, myoclonus, rotator cuff syndrome, tremor, urinary tract infection, . NAMENDA dosage: 10 MG BID PO. During the same period patient was treated with ARICEPT, CARAFATE, GLYBURIDE, NORVASC, KLONOPIN. Patient was hospitalized. Patient recovered.

Actira Side Effects Report #5610789-1
Physician from SPAIN reported ACTIRA problem on Jan 24, 2008. Male patient, 42 years of age, was diagnosed with sinusitis and was treated with ACTIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint effusion, rotator cuff syndrome, tendon rupture, . ACTIRA dosage: unknown. Patient recovered.