Menu

• Ask a Health Expert about ADDISON'S DISEASE
• Post Your Side Effect related to ADDISON'S DISEASE
• ADDISON'S DISEASE and FDA Warnings
• ADDISON'S DISEASE in Patients Wiki
• Report ADDISON'S DISEASE in Drug Side Effect Survey

ADDISON'S DISEASE side effect

What is ADDISON'S DISEASE ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Toprol Side Effects Report #5659547-2
Consumer or non-health professional from UNITED STATES reported TOPROL problem on Mar 10, 2008. Female patient, 57 years of age, weighting 110.0 lb, was diagnosed with migraine and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: addison's disease, asthenia, bradycardia, chest pain, dyspnoea, renal failure, syncope, . TOPROL dosage: 200MG 2PILLS 2X''S DAILY PO. Patient was hospitalized and became disabled. Patient recovered.

Toprol Side Effects Report #5660179-0
TOPROL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Female patient, 57 years of age, weighting 100.0 lb, was diagnosed with migraine and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: addison's disease, cardiac disorder, malaise, renal failure, . TOPROL dosage: 200 MG. 4 X DAILY PO. Patient was hospitalized. Patient recovered.

Amevive Side Effects Report #5688046-7
Health Professional from UNITED STATES reported AMEVIVE problem on Mar 12, 2008. Female patient, 69 years of age, weighting 229.9 lb, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: addison's disease, hypothyroidism, ileus, influenza like illness, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. Patient was hospitalized. Patient recovered.

Prednisone Side Effects Report #5626296-6
PREDNISONE problem was reported by a Health Professional from UNITED STATES on Feb 13, 2008. Female patient, 31 years of age, weighting 160.0 lb, was diagnosed with angioplasty, pericarditis, post procedural complication and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: addison's disease, asthenia, autonomic nervous system imbalance, blood insulin increased, diplopia, dizziness, glucose tolerance impaired, headache, hypoglycaemia, . PREDNISONE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.


Lepirudin Side Effects Report #5594452-1
Health Professional from FRANCE reported LEPIRUDIN problem on Jan 03, 2008. Male patient, 33 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with LEPIRUDIN. After drug was administered, patient experienced the following problems/side effects: addison's disease, adrenal haemorrhage, asthenia, confusional state, diarrhoea, pyrexia, . LEPIRUDIN dosage: unknown. Patient recovered.

Sandostatin Side Effects Report #5527484-X
SANDOSTATIN problem was reported by a Pharmacist from UNITED KINGDOM on Nov 23, 2007. Female patient, 44 years of age, was diagnosed with fistula discharge, pain, nausea, prophylaxis against gastrointestinal ulcer, lower respiratory tract infection and was treated with SANDOSTATIN. After drug was administered, patient experienced the following problems/side effects: addison's disease, hyperkalaemia, hyponatraemia, malignant neoplasm progression, renal failure, . SANDOSTATIN dosage: unknown. During the same period patient was treated with DIAMORPHINE, CYCLIZINE, OMEPRAZOLE, FENTANYL, LOPERAMIDE, DEXAMETHASONE, PARACETAMOL, CEFACLOR. Patient died on 11/14/2007.

Vancomycin Side Effects Report #5503938-7
Health Professional from UNITED STATES reported VANCOMYCIN problem on Oct 30, 2007. Male patient, 45 years of age, weighting 210.0 lb, was diagnosed with post procedural infection and was treated with VANCOMYCIN. After drug was administered, patient experienced the following problems/side effects: addison's disease, cardiac disorder, dyspnoea, hearing impaired, post procedural infection, rash, red man syndrome, . VANCOMYCIN dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5472209-X
REBIF problem was reported by a Physician from UNITED STATES on Sept 12, 2007. Male patient, 35 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: addison's disease, adrenocortical insufficiency acute, deafness transitory, deafness unilateral, ear haemorrhage, fall, orthostatic hypotension, skull fracture, . REBIF dosage: unknown. During the same period patient was treated with TYLENOL, INSULIN PUMP. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5405819-6
Consumer or non-health professional from UNITED STATES reported REBIF problem on July 24, 2007. Male patient, 35 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: addison's disease, . REBIF dosage: unknown. During the same period patient was treated with TYLENOL, INSULIN PUMP. Patient recovered.


Rebif Side Effects Report #5422953-5
REBIF problem was reported by a Physician from UNITED STATES on Aug 07, 2007. Male patient, 35 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: addison's disease, deafness transitory, deafness unilateral, ear haemorrhage, fall, fatigue, loss of consciousness, skull fracture, . REBIF dosage: unknown. During the same period patient was treated with TYLENOL, INSULIN PUMP. Patient was hospitalized. Patient recovered.

Diphenhydramine Side Effects Report #5381798-5
Pharmacist from UNITED STATES reported DIPHENHYDRAMINE problem on July 05, 2007. Female patient, weighting 145.3 lb, was treated with DIPHENHYDRAMINE. After drug was administered, patient experienced the following problems/side effects: addison's disease, anxiety, condition aggravated, feeling abnormal, nervousness, restlessness, . DIPHENHYDRAMINE dosage: 25MG PREMED Q4WEEKS IV. Patient recovered.

Danaparoid Side Effects Report #5400206-9
DANAPAROID problem was reported by a Consumer or non-health professional from GERMANY on July 10, 2007. Male patient, 33 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with DANAPAROID. After drug was administered, patient experienced the following problems/side effects: addison's disease, adrenal haemorrhage, anorexia, asthenia, back pain, confusional state, diarrhoea, inflammation, injection site erythema, . DANAPAROID dosage: unknown. During the same period patient was treated with HEPARIN. Patient was hospitalized. Patient recovered.

Diphenhydramine Side Effects Report #5381798-5
Pharmacist from UNITED STATES reported DIPHENHYDRAMINE problem on July 05, 2007. Female patient, weighting 145.3 lb, was treated with DIPHENHYDRAMINE. After drug was administered, patient experienced the following problems/side effects: addison's disease, anxiety, condition aggravated, feeling abnormal, nervousness, restlessness, . DIPHENHYDRAMINE dosage: 25MG PREMED Q4WEEKS IV. Patient recovered.

Danaparoid Side Effects Report #5400206-9
DANAPAROID problem was reported by a Consumer or non-health professional from GERMANY on July 10, 2007. Male patient, 33 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with DANAPAROID. After drug was administered, patient experienced the following problems/side effects: addison's disease, adrenal haemorrhage, anorexia, asthenia, back pain, confusional state, diarrhoea, inflammation, injection site erythema, . DANAPAROID dosage: unknown. During the same period patient was treated with HEPARIN. Patient was hospitalized. Patient recovered.


Atorvastatin Side Effects Report #5793107-8
Pharmacist from UNITED STATES reported ATORVASTATIN CALCIUM problem on June 26, 2008. Male patient, 81 years of age, weighting 116.8 lb, was diagnosed with hyperlipidaemia and was treated with ATORVASTATIN CALCIUM. After drug was administered, patient experienced the following problems/side effects: addison's disease, collagen-vascular disease, eosinophilia, hypersensitivity, infection parasitic, neoplasm, . ATORVASTATIN CALCIUM dosage: 20 MG EVERY DAY PO. Patient recovered.

Evista Side Effects Report #5732479-7
EVISTA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 24, 2008. Female patient, 74 years of age, was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: addison's disease, asthenia, bronchitis, cystitis, diarrhoea, nausea, . EVISTA dosage: unknown. During the same period patient was treated with CHOLESTYRAMINE, HYDROCORTISONE. Patient recovered.

Byetta Side Effects Report #5749925-5
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 19, 2008. Female patient, weighting 180.0 lb, was diagnosed with type 2 diabetes mellitus, sciatica and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: addison's disease, asthenia, blood potassium increased, decreased appetite, fatigue, hyperhidrosis, hyperventilation, injection site bruising, injection site haemorrhage, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ASPIRIN, LIPITOR, LYRICA. Patient was hospitalized. Patient recovered.

Nasonex Side Effects Report #5751702-6
NASONEX problem was reported by a Physician from UNITED STATES on May 15, 2008. Female patient was treated with NASONEX. After drug was administered, patient experienced the following problems/side effects: addison's disease, . NASONEX dosage: unknown. During the same period patient was treated with FLOVENT. Patient recovered.

Byetta Side Effects Report #5752208-0
Consumer or non-health professional from UNITED STATES reported BYETTA problem on May 23, 2008. Female patient, weighting 180.0 lb, was diagnosed with type 2 diabetes mellitus, blood cholesterol increased, sciatica and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: addison's disease, asthenia, blood potassium increased, decreased appetite, fatigue, hyperhidrosis, hyperventilation, injection site bruising, injection site haemorrhage, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ASPIRIN, LIPITOR, LYRICA. Patient was hospitalized. Patient recovered.


Ortho Side Effects Report #5708209-1
ORTHO TRI problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 09, 2008. Female patient, weighting 110.0 lb, was diagnosed with contraception and was treated with ORTHO TRI. After drug was administered, patient experienced the following problems/side effects: addison's disease, . ORTHO TRI dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5721274-0
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Apr 18, 2008. Female patient, weighting 120.0 lb, was diagnosed with pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: addison's disease, application site rash, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient recovered.

Interferon Side Effects Report #5370312-6
INTERFERON ALFA problem was reported by a Health Professional from JAPAN on June 15, 2007. Male patient, 47 years of age, weighting 115.7 lb, was treated with INTERFERON ALFA. After drug was administered, patient experienced the following problems/side effects: addison's disease, . INTERFERON ALFA dosage: unknown. During the same period patient was treated with INTERFERON ALFA. Patient was hospitalized. Patient recovered.

Cortef Side Effects Report #5322765-7
Consumer or non-health professional from UNITED STATES reported CORTEF problem on Apr 30, 2007. Female patient, weighting 162.0 lb, was diagnosed with addison's disease and was treated with CORTEF. After drug was administered, patient experienced the following problems/side effects: addison's disease, bone density decreased, lethargy, . CORTEF dosage: unknown. During the same period patient was treated with PREDNISONE, TOPROL, FLORINEF, SYNTHROID, METOPROLOL SUCCINATE, AVAPRO, ZOCOR, ACETYLSALICYLIC ACID SRT. Patient recovered.

Dexamethasone Side Effects Report #5326907-9
DEXAMETHASONE problem was reported by a Consumer or non-health professional from NETHERLANDS on May 03, 2007. Male patient, 74 years of age, was treated with DEXAMETHASONE. After drug was administered, patient experienced the following problems/side effects: addison's disease, arteriosclerosis coronary artery, cardiac arrest, cardiac disorder, chest pain, dyspnoea, hyperhidrosis, musculoskeletal pain, pain in extremity, . DEXAMETHASONE dosage: unknown. Patient died.

Natalizumab Side Effects Report #5328224-X
Physician from UNITED STATES reported NATALIZUMAB problem on May 01, 2007. Female patient, 34 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: addison's disease, bacteria urine identified, coma, condition aggravated, confusional state, delusion, depressed mood, encephalopathy, enterococcal infection, . NATALIZUMAB dosage: 300 MG QW IV. During the same period patient was treated with BACLOFEN, DETROL. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5670868-X
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 04, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, antiphospholipid syndrome, benign neoplasm, blood potassium decreased, bone density decreased, bronchitis, cerebellar atrophy, cerebellar infarction, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.

Seretide Side Effects Report #5612607-4
Physician from IRELAND reported SERETIDE problem on Jan 22, 2008. Female patient, 67 years of age, weighting 127.9 lb, was treated with SERETIDE. After drug was administered, patient experienced the following problems/side effects: acth stimulation test abnormal, addison's disease, blood cortisol decreased, contusion, skin atrophy, . SERETIDE dosage: unknown. During the same period patient was treated with STEROIDS, FLIXONASE, NEXIUM, SINGULAIR, VENTOLIN. Patient recovered.

Arixtra Side Effects Report #5595736-3
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Female patient, 48 years of age, weighting 238.5 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, addison's disease, adrenal haemorrhage, back pain, deep vein thrombosis, diarrhoea, disability, heparin-induced thrombocytopenia, myalgia, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with VICODIN, IMITREX, UROCIT, MAGNESIUM. Patient was hospitalized. Patient recovered.

Seretide Side Effects Report #5609661-2
Physician from IRELAND reported SERETIDE problem on Jan 22, 2008. Female patient, 47 years of age, weighting 127.9 lb, was treated with SERETIDE. After drug was administered, patient experienced the following problems/side effects: acth stimulation test abnormal, addison's disease, blood cortisol decreased, contusion, skin atrophy, . SERETIDE dosage: unknown. During the same period patient was treated with STEROIDS, FLIXONASE, NEXIUM, SINGULAIR, VENTOLIN. Patient recovered.

Desferal Side Effects Report #5453653-3
DESFERAL problem was reported by a Physician from UNITED STATES on Sept 05, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased, dyspepsia, nausea and was treated with DESFERAL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, chest pain, concomitant disease progression, constipation, cough, . DESFERAL dosage: 2200 MG, QD. During the same period patient was treated with NEXIUM, ZOFRAN. Patient was hospitalized. Patient recovered.

Desferal Side Effects Report #5404039-9
Physician from UNITED STATES reported DESFERAL T problem on July 23, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased, dyspepsia, nausea and was treated with DESFERAL T. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, chest pain, concomitant disease progression, constipation, cough, . DESFERAL T dosage: 2200 MG, QD. During the same period patient was treated with DESFERAL T, DESFERAL T, DESFERAL T, DESFERAL T, NEXIUM, ZOFRAN, EXJADE. Patient was hospitalized. Patient recovered.

Desferal Side Effects Report #5404040-5
DESFERAL T problem was reported by a Physician from UNITED STATES on July 23, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased, dyspepsia, nausea and was treated with DESFERAL T. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, aspartate aminotransferase increased, atelectasis, back pain, cellulitis, chest pain, concomitant disease progression, . DESFERAL T dosage: 2200 MG, QD. During the same period patient was treated with DESFERAL T, DESFERAL T, DESFERAL T, DESFERAL T, NEXIUM, ZOFRAN, EXJADE. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5375821-1
Physician from UNITED STATES reported EXJADE problem on June 21, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, concomitant disease progression, constipation, dehydration, diarrhoea, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5394983-3
EXJADE problem was reported by a Physician from UNITED STATES on July 13, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, chest pain, concomitant disease progression, constipation, dehydration, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5375821-1
Physician from UNITED STATES reported EXJADE problem on June 21, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, concomitant disease progression, constipation, dehydration, diarrhoea, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5394983-3
EXJADE problem was reported by a Physician from UNITED STATES on July 13, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, chest pain, concomitant disease progression, constipation, dehydration, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5747857-X
Physician from UNITED STATES reported FOSAMAX problem on May 14, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis, systemic lupus erythematosus and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, antiphospholipid syndrome, arthropathy, benign neoplasm, blood potassium decreased, bone density decreased, bronchitis, central nervous system lesion, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.

Florinef Side Effects Report #5344110-3
FLORINEF problem was reported by a Consumer or non-health professional from SPAIN on May 21, 2007. Female patient was treated with FLORINEF. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, addison's disease, anorexia, asthenia, blood potassium increased, blood pressure decreased, dehydration, grand mal convulsion, . FLORINEF dosage: .15 MG, QD. During the same period patient was treated with LITHIUM CARBONATE, PERICIAZINE, LORAZEPAM, HYDROCORTISONE. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5352058-3
Physician from UNITED STATES reported EXJADE problem on May 29, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, ankle fracture, arthralgia, atelectasis, back pain, cellulitis, concomitant disease progression, constipation, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Florinef Side Effects Report #5355732-8
FLORINEF problem was reported by a Consumer or non-health professional from SPAIN on May 31, 2007. Female patient was treated with FLORINEF. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, addison's disease, anorexia, asthenia, blood potassium increased, blood pressure decreased, dehydration, dizziness, . FLORINEF dosage: .15 MG, QD. During the same period patient was treated with LITHIUM CARBONATE, PERICIAZINE, LORAZEPAM, HYDROCORTISONE. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5369906-3
Physician from SPAIN reported LITHIUM CARBONATE problem on June 08, 2007. Male patient, 29 years of age, was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, addison's disease, adrenocortical insufficiency acute, anorexia, asthenia, autoimmune disorder, condition aggravated, dehydration, dizziness, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with FLUDROCORTISONE ACETATE, PERICYAZINE, LORAZEPAM, HYDROCORTISONE, HALOPERIDOL, PREDNISONE. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5302897-X
EXJADE problem was reported by a Physician from UNITED STATES on Apr 06, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, concomitant disease progression, constipation, dehydration, diarrhoea, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Exjade Side Effects Report #5268021-7
Physician from UNITED STATES reported EXJADE problem on Mar 07, 2007. Female patient, 29 years of age, weighting 143.5 lb, was diagnosed with blood iron increased and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, addison's disease, arthralgia, back pain, cellulitis, concomitant disease progression, constipation, dehydration, diarrhoea, . EXJADE dosage: 1250 MG, QD. During the same period patient was treated with DESFERAL. Patient was hospitalized. Patient recovered.

Prednisone Side Effects Report #5272609-7
PREDNISONE problem was reported by a Health Professional from UNITED STATES on Mar 20, 2007. Female patient, 32 years of age, weighting 150.0 lb, was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, addison's disease, anxiety, bedridden, blood glucose decreased, blood glucose increased, diarrhoea, diplopia, dizziness, . PREDNISONE dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5664640-4
Physician from UNITED STATES reported FOSAMAX problem on Mar 04, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain, addison's disease, antiphospholipid syndrome, anxiety, benign hepatic neoplasm, benign neoplasm, blood potassium decreased, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5598482-5
FOSAMAX problem was reported by a Physician from UNITED STATES on Jan 15, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain, addison's disease, antiphospholipid syndrome, benign neoplasm, blood potassium decreased, bone density decreased, bronchitis, cerebellar atrophy, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE, NEURONTIN, PLAVIX, ASPIRIN, ADVAIR DISKUS, ALBUTEROL, MS CONTIN, TOPAMAX. Patient was hospitalized. Patient recovered.