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BLOOD PARATHYROID HORMONE INCREASED side effect

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Zometa Side Effects Report #5662469-4
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Mar 05, 2008. Male patient, 70 years of age, weighting 164.0 lb, was diagnosed with osteoporosis, prostate cancer and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone debridement, bone disorder, bone scan abnormal, colonic polyp, follicular thyroid cancer, gingival disorder, goitre, gynaecomastia, . ZOMETA dosage: unknown. During the same period patient was treated with THALIDOMIDE, LIPITOR, CELEBREX, PROSCAR, LUPRON, AREDIA, CARDURA, FOSAMAX. Patient recovered.

Cystagon Side Effects Report #5615916-8
CYSTAGON problem was reported by a Physician from FRANCE on Jan 17, 2008. Male patient, 21 years of age, was diagnosed with cystinosis and was treated with CYSTAGON. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, haemodialysis, haemoglobin decreased, laboratory test abnormal, peritoneal dialysis, peritoneal disorder, . CYSTAGON dosage: unknown. During the same period patient was treated with TAMOXIFEN. Patient was hospitalized. Patient recovered.

Alendronic Side Effects Report #5648362-1
Consumer or non-health professional from HONG KONG reported ALENDRONIC ACID problem on Feb 18, 2008. Female patient, 82 years of age, was diagnosed with osteoporosis and was treated with ALENDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone lesion, bone scan abnormal, creatinine renal clearance decreased, fall, femur fracture, hydroxyproline increased, low turnover osteopathy, pain in extremity, . ALENDRONIC ACID dosage: 70 MG WEEKLY ORAL. During the same period patient was treated with GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULPHATE, CALCIUM CARBONATE, VITAMIN D. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5594938-X
FOSAMAX problem was reported by a Physician from UNITED STATES on Jan 14, 2008. Male patient, 68 years of age, weighting 178.6 lb, was diagnosed with osteoporosis, benign prostatic hyperplasia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cholelithiasis, clostridium difficile colitis, colonic polyp, contusion, dehydration, depression, diarrhoea, dizziness, . FOSAMAX dosage: unknown. During the same period patient was treated with PROSCAR, HYTRIN, COZAAR, CARDURA. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5595866-6
Physician from UNITED STATES reported FOSAMAX problem on Jan 14, 2008. Male patient, 68 years of age, weighting 178.6 lb, was diagnosed with osteoporosis, benign prostatic hyperplasia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cholelithiasis, clostridium difficile colitis, colonic polyp, contusion, dehydration, depression, diarrhoea, dizziness, . FOSAMAX dosage: unknown. During the same period patient was treated with PROSCAR, HYTRIN, COZAAR, CARDURA. Patient was hospitalized. Patient recovered.

Coolm Side Effects Report #5575784-X
COOLM problem was reported by a Consumer or non-health professional from FRANCE on Dec 14, 2007. Female patient, 83 years of age, weighting 154.3 lb, was diagnosed with hypertension and was treated with COOLM. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bronchitis, cerebral atrophy, dyspnoea at rest, fall, hypercalcaemia, incontinence, malaise, superinfection, . COOLM dosage: 20/25MG (ONCE A DAY), ORAL. During the same period patient was treated with ATENOLOL, ACETYL, SERETIDE, CARBOCYSTEINE, TRIAMCINOLONE, LYSINE ACETYLSALICYLATE, LORAZEPAM. Patient was hospitalized. Patient recovered.

Dianeal Side Effects Report #5513096-0
Consumer or non-health professional from UNITED STATES reported DIANEAL problem on Nov 08, 2007. Male patient, 64 years of age, was diagnosed with renal failure chronic and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, multi-organ failure, poor peripheral circulation, . DIANEAL dosage: unknown. Patient was hospitalized. Patient died on 09/01/2007.

Zometa Side Effects Report #5521721-3
ZOMETA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 12, 2007. Male patient, 70 years of age, weighting 164.0 lb, was diagnosed with osteoporosis, prostate cancer and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone disorder, follicular thyroid cancer, goitre, hyperparathyroidism, parathyroid tumour benign, thyroidectomy, tooth extraction, wound debridement, . ZOMETA dosage: unknown. During the same period patient was treated with THALIDOMIDE, LIPITOR, CELEBREX, PROSCAR, LUPRON, AREDIA. Patient recovered.

Zometa Side Effects Report #5522086-3
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Nov 12, 2007. Male patient, 70 years of age, weighting 164.0 lb, was diagnosed with osteoporosis, prostate cancer and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone disorder, follicular thyroid cancer, goitre, hyperparathyroidism, parathyroid tumour benign, thyroidectomy, tooth extraction, wound debridement, . ZOMETA dosage: unknown. During the same period patient was treated with THALIDOMIDE, LIPITOR, CELEBREX, PROSCAR, LUPRON, AREDIA. Patient recovered.


Sustiva Side Effects Report #5491810-0
SUSTIVA problem was reported by a Health Professional from FRANCE on Oct 10, 2007. Male patient, 71 years of age, weighting 116.8 lb, was treated with SUSTIVA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, neuropathy, renal tubular disorder, vitamin d deficiency, . SUSTIVA dosage: unknown. During the same period patient was treated with ZERIT, VIDEX, KALETRA, VIREAD, PLAQUENIL, VIRLIX, TENORMIN, CORVASAL. Patient recovered.

Kaletra Side Effects Report #5495231-6
Health Professional from FRANCE reported KALETRA problem on Oct 15, 2007. Male patient, weighting 116.8 lb, was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone pain, hypophosphataemia, vitamin d deficiency, . KALETRA dosage: unknown. During the same period patient was treated with TENOFOVIR DISOPROXIL, EFAVIRENZ, HYDROXYCHLOROQUINE SULPHATE, RITONAVIR, CETIRIZINE, ATENOLOL, MOLSIDOMINE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5495360-7
FOSAMAX problem was reported by a Physician from UNITED STATES on Oct 18, 2007. Male patient, 68 years of age, weighting 178.6 lb, was diagnosed with osteoporosis, benign prostatic hyperplasia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cholelithiasis, clostridium difficile colitis, colonic polyp, contusion, dehydration, depression, diarrhoea, dizziness, . FOSAMAX dosage: unknown. During the same period patient was treated with PROSCAR, HYTRIN, COZAAR, CARDURA. Patient was hospitalized. Patient recovered.

Lansoprazole Side Effects Report #5500323-9
Consumer or non-health professional from JAPAN reported LANSOPRAZOLE problem on Oct 16, 2007. Female patient, 78 years of age, was diagnosed with gastric ulcer, helicobacter infection and was treated with LANSOPRAZOLE. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, electrocardiogram abnormal, hypercalcaemia, hyperkalaemia, hyperparathyroidism, parathyroid disorder, renal impairment, . LANSOPRAZOLE dosage: 30 MG (15 MG, 2 IN 1 D) PER ORAL. During the same period patient was treated with AMOXICILLIN TRIHYDRATE, CLARITHROMYCIN, RABEPRAZOLE, MAGNESIUM OXIDE, ETODOLAC, AZULENE SULFONATE. Patient was hospitalized. Patient recovered.

Lansoprazole Side Effects Report #5504294-0
LANSOPRAZOLE problem was reported by a Consumer or non-health professional from JAPAN on Oct 25, 2007. Female patient, 78 years of age, was diagnosed with gastric ulcer, helicobacter infection and was treated with LANSOPRAZOLE. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, electrocardiogram abnormal, helicobacter infection, hypercalcaemia, hyperkalaemia, hyperparathyroidism primary, parathyroid disorder, renal impairment, . LANSOPRAZOLE dosage: 30 MG (15 MG,2 IN 1 D), PER ORAL. During the same period patient was treated with AMOXICILLIN TRIHYDRATE, CLARITHROMYCIN, RABEPRAZOLE, MAGNESIUM OXIDE, ETODOLAC. Patient was hospitalized. Patient recovered.


Mimpara Side Effects Report #5446097-1
Consumer or non-health professional from GERMANY reported MIMPARA problem on Aug 28, 2007. Female patient, 25 years of age, weighting 99.21 lb, was treated with MIMPARA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, gastric disorder, myalgia, nausea, skin disorder, . MIMPARA dosage: unknown. During the same period patient was treated with VITAMIN D, RENAGEL. Patient recovered.

Olmesartan Side Effects Report #5451029-6
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE problem was reported by a Health Professional from FRANCE on Aug 31, 2007. Female patient, 83 years of age, weighting 154.3 lb, was diagnosed with hypertension and was treated with OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, brain scan abnormal, bronchitis, fall, hypercalcaemia, incontinence, malaise, transient ischaemic attack, vitamin d decreased, . OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIZIDE dosage: 20/25MG (ONCE A DAY), ORAL. During the same period patient was treated with ATENOLOL, ACETYL, SERETIDE, CARBOCYSTEINE, TRIAMCINOLONE, LYSINE ACETYLSALICYLATE, LORAZEPAM. Patient was hospitalized. Patient recovered.

Reclast Side Effects Report #5469276-6
Physician from BRAZIL reported RECLAST problem on Sept 18, 2007. Male patient was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, calcium ionised decreased, . RECLAST dosage: 5MG/100ML. Patient recovered.

Rocaltrol Side Effects Report #5418211-5
ROCALTROL problem was reported by a Health Professional from UNITED STATES on Aug 07, 2007. Male patient, child 3 years of age, weighting 28.66 lb, was diagnosed with hyperparathyroidism and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, therapeutic product contamination, . ROCALTROL dosage: unknown. During the same period patient was treated with FERROUS SULPHATE. Patient recovered.

Renagel Side Effects Report #5422044-3
Consumer or non-health professional from UNITED STATES reported RENAGEL problem on Aug 06, 2007. Female patient was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, dry throat, foreign body trauma, . RENAGEL dosage: unknown. Patient recovered.


Diclofenac Side Effects Report #5434323-4
DICLOFENAC problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Aug 16, 2007. Female patient, 65 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, hyperkalaemia, hypoaldosteronism, hyponatraemia, kidney enlargement, metabolic acidosis, nephrolithiasis, pneumonia, . DICLOFENAC dosage: 150 MG (50 MG, 3 IN 1 D). Patient was hospitalized. Patient died.

Rocaltrol Side Effects Report #5378611-9
Consumer or non-health professional from UNITED STATES reported ROCALTROL problem on June 27, 2007. Male patient, child 3 years of age, was diagnosed with hyperparathyroidism and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, therapeutic product contamination, . ROCALTROL dosage: unknown. During the same period patient was treated with FERROUS SULPHATE. Patient recovered.

Rocaltrol Side Effects Report #5390212-5
ROCALTROL problem was reported by a Health Professional from UNITED STATES on July 10, 2007. Male patient, child 3 years of age, weighting 28.88 lb, was diagnosed with hyperparathyroidism and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, therapeutic product contamination, . ROCALTROL dosage: unknown. During the same period patient was treated with FERROUS SULPHATE. Patient recovered.

Epogen Side Effects Report #5398735-X
Health Professional from UNITED STATES reported EPOGEN problem on Nov 20, 2006. Male patient, 48 years of age, was diagnosed with dialysis, hyperparathyroidism secondary and was treated with EPOGEN. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, haemoglobin decreased, . EPOGEN dosage: unknown. During the same period patient was treated with SENSIPAR, TOPROL, PREVACID, MAGNESIUM OXIDE, LASIX, AVAPRO, RENAX, NORVASC. Patient recovered.

Rocaltrol Side Effects Report #5378611-9
ROCALTROL problem was reported by a Consumer or non-health professional from UNITED STATES on June 27, 2007. Male patient, child 3 years of age, was diagnosed with hyperparathyroidism and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, therapeutic product contamination, . ROCALTROL dosage: unknown. During the same period patient was treated with FERROUS SULPHATE. Patient recovered.

Rocaltrol Side Effects Report #5390212-5
Health Professional from UNITED STATES reported ROCALTROL problem on July 10, 2007. Male patient, child 3 years of age, weighting 28.88 lb, was diagnosed with hyperparathyroidism and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, therapeutic product contamination, . ROCALTROL dosage: unknown. During the same period patient was treated with FERROUS SULPHATE. Patient recovered.

Epogen Side Effects Report #5398735-X
EPOGEN problem was reported by a Health Professional from UNITED STATES on Nov 20, 2006. Male patient, 48 years of age, was diagnosed with dialysis, hyperparathyroidism secondary and was treated with EPOGEN. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, haemoglobin decreased, . EPOGEN dosage: unknown. During the same period patient was treated with SENSIPAR, TOPROL, PREVACID, MAGNESIUM OXIDE, LASIX, AVAPRO, RENAX, NORVASC. Patient recovered.

Zemplar Side Effects Report #5756002-6
Consumer or non-health professional from UNITED STATES reported ZEMPLAR problem on Apr 09, 2008. Female patient was treated with ZEMPLAR. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, . ZEMPLAR dosage: unknown. Patient recovered.

Rasilez Side Effects Report #5782416-4
RASILEZ problem was reported by a Consumer or non-health professional from GERMANY on June 10, 2008. Female patient was diagnosed with hypertension, depression and was treated with RASILEZ. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, blood pressure inadequately controlled, blood pressure increased, blood pressure systolic increased, hypertensive crisis, renin increased, . RASILEZ dosage: 75 MG/D. During the same period patient was treated with TREVILOR, DELIX, DOXAZOSIN MESYLATE, DOXAZOSIN MESYLATE. Patient recovered.

Vitamin Side Effects Report #5792552-4
Consumer or non-health professional from CANADA reported VITAMIN D2 problem on June 09, 2008. Female patient, 77 years of age, was treated with VITAMIN D2. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, hypercalcaemia, . VITAMIN D2 dosage: unknown. Patient recovered.

Evista Side Effects Report #5725059-0
EVISTA problem was reported by a Health Professional from JAPAN on Apr 21, 2008. Female patient was diagnosed with osteoporosis and was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, . EVISTA dosage: 60 MG, DAILY (1/D). During the same period patient was treated with THYRADIN S, ASPIRIN, MERISLON, FLUNITRAZEPAM, NORVASC, FUROSEMIDE, OMEPRAZOLE. Patient recovered.

Seroquel Side Effects Report #5733192-2
Consumer or non-health professional from UNITED STATES reported SEROQUEL problem on Apr 24, 2008. Male patient, 40 years of age, weighting 220.0 lb, was diagnosed with sleep disorder, anxiety, depression and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, hallucination, auditory, hypoaesthesia, nephrolithiasis, paraesthesia, somnolence, speech disorder, . SEROQUEL dosage: unknown. During the same period patient was treated with DESERIL. Patient recovered.

Hydrochlorothiaz Side Effects Report #5737240-5
HYDROCHLOROTHIAZIDE problem was reported by a Health Professional from FRANCE on May 07, 2008. Female patient, 69 years of age, weighting 119.0 lb, was treated with HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, creatinine urine decreased, hypercalcaemia, urine osmolarity decreased, . HYDROCHLOROTHIAZIDE dosage: 75 MG/DAY. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5699917-X
Physician from UNITED STATES reported FOSAMAX problem on Apr 02, 2008. Male patient, 68 years of age, weighting 178.6 lb, was diagnosed with osteoporosis, benign prostatic hyperplasia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cholelithiasis, clostridium difficile colitis, colonic polyp, contusion, decreased appetite, dehydration, depression, diarrhoea, . FOSAMAX dosage: unknown. During the same period patient was treated with PROSCAR, HYTRIN, COZAAR, CARDURA. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5719829-2
FOSAMAX problem was reported by a Physician from UNITED STATES on Apr 16, 2008. Male patient, 68 years of age, weighting 178.6 lb, was diagnosed with osteoporosis, benign prostatic hyperplasia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cholelithiasis, clostridium difficile colitis, colonic polyp, contusion, decreased appetite, dehydration, depression, diarrhoea, . FOSAMAX dosage: unknown. During the same period patient was treated with PROSCAR, HYTRIN, COZAAR, CARDURA. Patient was hospitalized. Patient recovered.

Isotretinoin Side Effects Report #5724559-7
Consumer or non-health professional from JAPAN reported ISOTRETINOIN problem on Apr 10, 2008. Male patient, child 3 years of age, was diagnosed with neuroblastoma and was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, blood urea increased, creatinine renal clearance decreased, hypercalcaemia, pneumonia fungal, . ISOTRETINOIN dosage: 130 MG/M**2;, 130 MG/M**2;. During the same period patient was treated with VINCRISTINE, CYCLOPHOSPHAMIDE, DOXORUBICIN, CISPLATIN, ETOPOSIDE, MELPHALAN, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Hectorol Side Effects Report #5362849-0
HECTOROL problem was reported by a Physician from UNITED STATES on June 07, 2007. Male patient, 79 years of age, was diagnosed with hyperparathyroidism secondary and was treated with HECTOROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cardiac disorder, dizziness, hyperhidrosis, paranoia, pruritus, . HECTOROL dosage: unknown. During the same period patient was treated with ZEMPLAR, CALCITRIOL. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5371018-X
Consumer or non-health professional from CANADA reported FORTEO problem on June 13, 2007. Male patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, parathyroid tumour, . FORTEO dosage: unknown. Patient recovered.

Rocaltrol Side Effects Report #5372147-7
ROCALTROL problem was reported by a Consumer or non-health professional from UNITED STATES on June 15, 2007. Male patient, child 3 years of age, was diagnosed with hyperparathyroidism and was treated with ROCALTROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, therapeutic product contamination, . ROCALTROL dosage: unknown. During the same period patient was treated with FERROUS SULPHATE. Patient recovered.

Hectorol Side Effects Report #5341031-7
Consumer or non-health professional from UNITED STATES reported HECTOROL problem on May 16, 2007. Male patient, 79 years of age, was diagnosed with hyperparathyroidism secondary and was treated with HECTOROL. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, cardiac disorder, dizziness, hyperhidrosis, pruritus, . HECTOROL dosage: unknown. During the same period patient was treated with ZEMPLAR, CALCITRIOL. Patient was hospitalized. Patient recovered.

Zemplar Side Effects Report #5294754-2
ZEMPLAR problem was reported by a Physician from GERMANY on Apr 03, 2007. Female patient, 58 years of age, was treated with ZEMPLAR. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, . ZEMPLAR dosage: unknown. Patient recovered.

Pamidronate Side Effects Report #5298625-7
Health Professional from UNITED KINGDOM reported PAMIDRONATE DI problem on Apr 11, 2007. Female patient, 56 years of age, was diagnosed with multiple myeloma and was treated with PAMIDRONATE DI. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone disorder, fibrosis, high turnover osteopathy, hyperparathyroidism secondary, hypocalcaemia, malignant neoplasm progression, osteoprotegerin ligand, renal impairment, . PAMIDRONATE DI dosage: unknown. During the same period patient was treated with THALIDOMIDE. Patient died.

Sensipar Side Effects Report #5298835-9
SENSIPAR problem was reported by a Health Professional from UNITED STATES on Sept 15, 2004. Male patient, 58 years of age, was diagnosed with hyperparathyroidism secondary, dialysis and was treated with SENSIPAR. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, rash erythematous, . SENSIPAR dosage: unknown. During the same period patient was treated with HECTORAL, RENAGEL, VENOFER, EPOGEN, NEXIUM, ASPIRIN, LIPITOR, CLONAZEPAM. Patient recovered.

Sensipar Side Effects Report #5301002-3
Physician from UNITED STATES reported SENSIPAR problem on Jan 30, 2007. Male patient, 55 years of age, was diagnosed with hyperparathyroidism secondary and was treated with SENSIPAR. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, . SENSIPAR dosage: unknown. During the same period patient was treated with SEVELAMER, ROCALTROL. Patient recovered.

Sensipar Side Effects Report #5301005-9
SENSIPAR problem was reported by a Physician from UNITED STATES on Jan 30, 2007. Male patient, 56 years of age, was diagnosed with hyperparathyroidism secondary and was treated with SENSIPAR. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, . SENSIPAR dosage: unknown. Patient recovered.

Cymbalta Side Effects Report #5227594-0
Physician from UNITED STATES reported CYMBALTA problem on Oct 20, 2006. Female patient, 56 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, . CYMBALTA dosage: 30 MG. Patient recovered.

Zemplar Side Effects Report #5264263-5
ZEMPLAR problem was reported by a Physician from GERMANY on Mar 05, 2007. Male patient, weighting 251.3 lb, was diagnosed with hyperparathyroidism secondary, diabetes mellitus and was treated with ZEMPLAR. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, parathyroidectomy, . ZEMPLAR dosage: unknown. During the same period patient was treated with ANTIPHOSPHATE, INSULIN, CLOPIDOGREL BISULPHATE, RAMIPRIL, AMLODIPINE, FUROSEMIDE, CARVEDILOL. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5673303-0
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Mar 06, 2008. Female patient, 78 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood calcium increased, blood parathyroid hormone increased, dizziness, loss of consciousness, . FORTEO dosage: unknown. During the same period patient was treated with REMICADE, PREDNISONE, IMMUNOSUPPRESSIVE AGENTS. Patient recovered.

Nexavar Side Effects Report #5625714-7
NEXAVAR problem was reported by a Physician from NETHERLANDS on Feb 11, 2008. Female patient was diagnosed with follicular thyroid cancer, routine health maintenance and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, blood parathyroid hormone increased, hypocalcaemia, mucosal inflammation, palmar-plantar erythrodysaesthesia syndrome, pneumothorax, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG. During the same period patient was treated with DIETARY SUPPLEMENTS. Patient recovered.

Trileptal Side Effects Report #5599711-4
Consumer or non-health professional from FRANCE reported TRILEPTAL problem on Jan 17, 2008. Female patient, 44 years of age, weighting 174.2 lb, was diagnosed with neuralgia, rheumatoid arthritis, adrenal insufficiency and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood parathyroid hormone increased, blood phosphorus decreased, hyperparathyroidism secondary, hypocalcaemia, muscle spasms, urine calcium increased, vitamin d decreased, . TRILEPTAL dosage: 120 MG, BID. During the same period patient was treated with PROPOFAN, LAROXYL, LIDOCAINE, METHOTREXATE, LEDERFOLIN, CORTANCYL, HYDROCORTISONE, FLUDROCORTISONE ACETATE. Patient recovered.

Singulair Side Effects Report #5604455-6
SINGULAIR problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 23, 2008. Female patient, 52 years of age, weighting 165.0 lb, was diagnosed with sinusitis, gastrooesophageal reflux disease and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: arthralgia, blood parathyroid hormone increased, choking, gastrooesophageal reflux disease, lethargy, osteopenia, osteoporosis, parathyroid tumour benign, . SINGULAIR dosage: unknown. During the same period patient was treated with PROTONIX. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5570776-9
Physician from CANADA reported FORTEO problem on Dec 11, 2007. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: arthralgia, blood parathyroid hormone increased, oedema peripheral, systemic lupus erythematosus, vitamin d decreased, . FORTEO dosage: unknown. During the same period patient was treated with METHOTREXATE, NAPROSYN, LOSEC, ADALAT, VITAMIN B, CALCIUM. Patient recovered.