ILL-DEFINED DISORDER side effect
What is ILL-DEFINED DISORDER ?Drugs associated with ILL-DEFINED DISORDER
ABREVA ACCUTANE ACTOPLUS ACYCLOVIR ADALAT ADVAIR ADVICOR ALBUTEROL ALENDRONATE ALEVE ALPRAZOLAM ALTABAX AMBIEN AMIODARONE AMOXICILLIN APIDRA ARIMIDEX ARIXTRA ATIVAN AUGMENTIN AVANDAMET AVANDIA AVELOX AVODART AVONEX AZULFIDINE BACTRIM BENADRYL BENICAR BETAMETHASONE BONDRONAT BONIVA BUDEPRION BUPIVACAINE BUPROPION CARBAMAZEPINE CHAMPIX CHANTIX CIPROFLOXACIN CISPLATIN CLARITHROMYCIN CLOMID COMMIT COREG CRESTOR DEXEDRINE DILANTIN DILATREND DITROPAN EFFEXOR ELIDEL ENALAPRIL ERBITUX ESCITALOPRAM EXUBERA FABRAZYME FELODIPINE FLAGYL FLOLAN FLONASE FLORINEF FLUDARABINE FLUOROURACIL FLUOXETINE FLUTICASONE FORTEO GADOLINIUM GEODON GLUCOPHAGE HUMIRA HYDROCHLOROTHIAZ HYPERTONIC IBANDRONIC IFOSFAMIDE IMITREX INTRON ISOTRETINOIN JANUVIA KEPPRA KETEK KLONOPIN LAMICTAL LAMIVUDINE LAPATINIB LEVAQUIN LEVITRA LEXAPRO LIORESAL LIPITOR LISINOPRIL LITHIUM LOVASTATIN LUNESTA LYRICA MELLARIL METHOTREXATE MIDAZOLAM MINOXIDIL MIRAPEX MIRCERA MORPHINE NATALIZUMAB NEOSTIGMINE NEUPRO NEXAVAR NIASPAN NICORETTE NIMOTOP ONDANSETRON ORLISTAT PAROXETINE PAXIL PAZOPANIB PERIOCHIP PHENYTOIN PLAVIX PREDNISONE PRIALT PRIMATENE PROAIR PROGRAF PROMETHAZINE PROVENTIL PROVIGIL RABEPRAZOLE REBIF RELENZA REQUIP REVLIMID RISPERDAL RISPERIDONE RITALIN ROACCUTANE ROACUTAN SERETIDE SEREVENT SEROQUEL SERTRALINE SIMVASTATIN SINGULAIR SORIATANE SPIRIVA STAVUDINE STILNOX SULFAMETHOXAZOLE SYMBICORT TAHOR TAMSULOSIN TEGRETOL TEMODAL TEMOZOLOMIDE THALIDOMIDE THALOMID THERAFLU TOPAMAX TRIAMTERENE TYKERB TYSABRI VALACYCLOVIR VALPROATE VALTREX VECURONIUM VENTOLIN VERAMYST VIOXX VYTORIN WELLBUTRIN XANAX XELODA XENICAL XOPENEX ZANTAC ZESTRIL ZIDOVUDINE ZOFRAN ZOLPIDEM ZOMIG ZOSYN ZYPREXA ZYRTECILL-DEFINED DISORDER : Ditropan Side Effects Report #5652376-5
Health Professional from UNITED STATES reported DITROPAN problem on Mar 05, 2008. Female patient was diagnosed with cystitis interstitial and was treated with DITROPAN. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . DITROPAN dosage: 10MG. Patient recovered.
ILL-DEFINED DISORDER : Requip Side Effects Report #5654845-0
REQUIP problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 08, 2007. Female patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . REQUIP dosage: 3MG PER DAY. Patient recovered.
ILL-DEFINED DISORDER : Requip Side Effects Report #5654929-7
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Sept 12, 2007. Female patient, 74 years of age, was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, restless legs syndrome, . REQUIP dosage: .25MG PER DAY. During the same period patient was treated with PREDNISOLONE. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659261-3
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on June 14, 2007. Male patient, 23 years of age, weighting 269.0 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659278-9
Consumer or non-health professional from UNITED STATES reported ALEVE problem on June 16, 2007. Female patient, 26 years of age, weighting 174.2 lb, was diagnosed with toothache and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . ALEVE dosage: TOTAL DAILY DOSE: 1760 MG UNIT DOSE: 220 MG. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659280-7
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on June 13, 2007. Male patient, child 3 years of age, weighting 33.07 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659309-6
Consumer or non-health professional from UNITED STATES reported ALEVE problem on June 24, 2007. Female patient, 16 years of age, weighting 165.3 lb, was diagnosed with dysmenorrhoea and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: UNIT DOSE: 220 MG. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659701-X
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on July 02, 2007. Male patient, 32 years of age, weighting 262.4 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with MORPHINE. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659702-1
Consumer or non-health professional from UNITED STATES reported ALEVE problem on June 22, 2007. Male patient, 72 years of age, weighting 291.0 lb, was diagnosed with neuralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: TOTAL DAILY DOSE: 1760 MG UNIT DOSE: 220 MG. During the same period patient was treated with GLUCOPHAGE, GLIPIZIDE, TENORMIN, ZOCOR, TOPROL, VICODIN, MOTRIN. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659729-X
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 25 years of age, weighting 220.5 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: UNIT DOSE: 220 MG. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659758-6
Consumer or non-health professional from UNITED STATES reported ALEVE problem on July 09, 2007. Male patient, 52 years of age, weighting 335.1 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG. During the same period patient was treated with METHOCARBAMOL. Patient recovered.
ILL-DEFINED DISORDER : Aleve Side Effects Report #5659760-4
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2007. Female patient, 42 years of age, weighting 121.3 lb, was diagnosed with pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, no adverse event, . ALEVE dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, ZOCOR. Patient recovered.
ILL-DEFINED DISORDER : Fluorouracil Side Effects Report #5671999-0
Consumer or non-health professional from UNITED STATES reported FLUOROURACIL problem on Mar 17, 2008. Female patient, 73 years of age, weighting 150.0 lb, was diagnosed with vulval cancer and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, malaise, . FLUOROURACIL dosage: unknown. During the same period patient was treated with CISPLATIN. Patient was hospitalized. Patient died on 03/22/2007.
ILL-DEFINED DISORDER : Methotrexate Side Effects Report #5675682-7
METHOTREXATE problem was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Mar 05, 2008. Female patient, 60 years of age, was diagnosed with central nervous system lymphoma and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, muscular weakness, myelopathy, sensory disturbance, sepsis, spinal cord disorder, therapeutic agent toxicity, urinary incontinence, vibration test abnormal, . METHOTREXATE dosage: 12 MG INTRATHECAL; 1 G/M2 INTRAVENOUS. During the same period patient was treated with CYTARABINE, HYDROCORTISONE. Patient died.
ILL-DEFINED DISORDER : Zyrtec Side Effects Report #5675765-1
Consumer or non-health professional from UNITED STATES reported ZYRTEC problem on Mar 10, 2008. Female patient, 54 years of age, weighting 400.0 lb, was diagnosed with hypersensitivity and was treated with ZYRTEC. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, respiratory arrest, . ZYRTEC dosage: 1 IR TABLET DAILY (10 MG), ORAL. Patient was hospitalized. Patient recovered.
ILL-DEFINED DISORDER : Plavix Side Effects Report #5675996-0
PLAVIX problem was reported by a Physician from FRANCE on Mar 12, 2008. Male patient was diagnosed with cardiovascular disorder and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, refractory anaemia, . PLAVIX dosage: unknown. During the same period patient was treated with TAHOR. Patient was hospitalized. Patient died.
ILL-DEFINED DISORDER : Stavudine Side Effects Report #5677438-8
Health Professional from UNITED KINGDOM reported STAVUDINE problem on Mar 20, 2008. Male patient, 69 years of age, was diagnosed with hiv infection and was treated with STAVUDINE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, malignant melanoma, metastases to lymph nodes, metastases to skin, neoplasm malignant, . STAVUDINE dosage: unknown. During the same period patient was treated with INDINIVIR SULPHATE, NEVIRAPINE, RITONAVIR. Patient died on 01/01/2005.
ILL-DEFINED DISORDER : Nimotop Side Effects Report #5678016-7
NIMOTOP problem was reported by a Pharmacist from UNITED STATES on Mar 24, 2008. Female patient, 65 years of age, was diagnosed with subarachnoid haemorrhage and was treated with NIMOTOP. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . NIMOTOP dosage: 60MG Q4H PO. Patient was hospitalized. Patient recovered.
ILL-DEFINED DISORDER : Enalapril Side Effects Report #5678104-5
Consumer or non-health professional from UNITED STATES reported ENALAPRIL MALEATE problem on Mar 24, 2008. Male patient, weighting 12.00 lb, was diagnosed with hypertension and was treated with ENALAPRIL MALEATE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, nervous system disorder, . ENALAPRIL MALEATE dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Geodon Side Effects Report #5684381-7
GEODON problem was reported by a Health Professional from UNITED STATES on Mar 27, 2008. Female patient, 43 years of age, weighting 130.0 lb, was diagnosed with schizophrenia, paranoid type and was treated with GEODON. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, tardive dyskinesia, tongue biting, . GEODON dosage: 80MG BID PO. Patient recovered.
ILL-DEFINED DISORDER : Mircera Side Effects Report #5684630-5
Physician from SWITZERLAND reported MIRCERA problem on Mar 18, 2008. Female patient, 57 years of age, weighting 266.8 lb, was treated with MIRCERA. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . MIRCERA dosage: unknown. During the same period patient was treated with CARVEDILOL, PHOSPHONORM, MIMPARA, NEXIUM, ROCALTROL, SINTROM, SORTIS, TEMESTA. Patient was hospitalized. Patient recovered.
ILL-DEFINED DISORDER : Chantix Side Effects Report #5690120-6
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 31, 2008. Male patient, 24 years of age, weighting 185.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, psychotic disorder, sleep phase rhythm disturbance, . CHANTIX dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Singulair Side Effects Report #5690588-5
Consumer or non-health professional from UNITED STATES reported SINGULAIR problem on Mar 31, 2008. Male patient, child 1 years of age, weighting 49.70 lb, was diagnosed with asthma and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, nervousness, . SINGULAIR dosage: unknown. Patient was hospitalized. Patient recovered.
ILL-DEFINED DISORDER : Singulair Side Effects Report #5690648-9
SINGULAIR problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 31, 2008. Female patient, child 6 years of age, weighting 40.00 lb, was diagnosed with asthma and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, psychomotor hyperactivity, suicidal ideation, . SINGULAIR dosage: 4 MG CHEWABLE DAILY. Patient recovered.
ILL-DEFINED DISORDER : Avonex Side Effects Report #5691237-2
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 18, 2008. Female patient was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, myocardial infarction, . AVONEX dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Theraflu Side Effects Report #5612458-0
THERAFLU problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Male patient, 47 years of age, weighting 185.0 lb, was treated with THERAFLU. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, pain, swelling, . THERAFLU dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
ILL-DEFINED DISORDER : Paxil Side Effects Report #5616626-3
Consumer or non-health professional from UNITED STATES reported PAXIL problem on Nov 12, 2007. Male patient, 30 years of age, was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . PAXIL dosage: 25MG PER DAY. During the same period patient was treated with CRESTOR, TRICOR. Patient recovered.
ILL-DEFINED DISORDER : Paroxetine Side Effects Report #5618183-4
PAROXETINE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 14, 2007. Female patient was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . PAROXETINE dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Avonex Side Effects Report #5619143-X
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Jan 25, 2008. Male patient, 52 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, surgery, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
ILL-DEFINED DISORDER : Spiriva Side Effects Report #5622776-8
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 15, 2008. Female patient was diagnosed with dyspnoea and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . SPIRIVA dosage: unknown. During the same period patient was treated with OXYGEN, WARFARIN, METOPROLOL TARTRATE, FOSINOPRIL, SIMVASTATIN. Patient recovered.
ILL-DEFINED DISORDER : Vioxx Side Effects Report #5626190-0
Consumer or non-health professional from UNITED STATES reported VIOXX problem on Feb 13, 2008. Female patient was diagnosed with arthralgia and was treated with VIOXX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, loss of consciousness, . VIOXX dosage: 25 MG. Patient was hospitalized and became disabled. Patient recovered.
ILL-DEFINED DISORDER : Ibandronic Side Effects Report #5629542-8
IBANDRONIC ACID problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 04, 2008. Female patient was treated with IBANDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . IBANDRONIC ACID dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Fabrazyme Side Effects Report #5631598-3
Consumer or non-health professional from UNITED STATES reported FABRAZYME problem on Feb 05, 2008. Male patient, 55 years of age, weighting 213.8 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . FABRAZYME dosage: unknown. Patient was hospitalized. Patient died on 02/02/2008.
ILL-DEFINED DISORDER : Humira Side Effects Report #5632176-2
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Female patient was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, knee arthroplasty, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.
ILL-DEFINED DISORDER : Felodipine Side Effects Report #5632427-4
Consumer or non-health professional from UNITED STATES reported FELODIPINE problem on Sept 17, 2007. Female patient was treated with FELODIPINE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, swelling, . FELODIPINE dosage: unknown. During the same period patient was treated with LISINOPRIL. Patient recovered.
ILL-DEFINED DISORDER : Lipitor Side Effects Report #5633432-4
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Male patient was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, walking aid user, . LIPITOR dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Zestril Side Effects Report #5634169-8
Consumer or non-health professional from UNITED STATES reported ZESTRIL problem on Feb 21, 2008. Male patient, weighting 190.0 lb, was diagnosed with hypertension and was treated with ZESTRIL. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . ZESTRIL dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Fluoxetine Side Effects Report #5636261-0
FLUOXETINE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Male patient, weighting 220.0 lb, was diagnosed with agoraphobia and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, nervous system disorder, . FLUOXETINE dosage: 20MG 1 PER DAY. Patient recovered.
ILL-DEFINED DISORDER : Veramyst Side Effects Report #5636380-9
Consumer or non-health professional from UNITED STATES reported VERAMYST problem on Nov 08, 2007. Male patient was diagnosed with sinus disorder and was treated with VERAMYST. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . VERAMYST dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Sertraline Side Effects Report #5637873-0
SERTRALINE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 22, 2008. Female patient, 64 years of age, weighting 170.0 lb, was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . SERTRALINE dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Primatene Side Effects Report #5639756-9
Consumer or non-health professional from UNITED STATES reported PRIMATENE MIST problem on Jan 29, 2008. Female patient was diagnosed with asthma and was treated with PRIMATENE MIST. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . PRIMATENE MIST dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Roaccutane Side Effects Report #5643117-6
ROACCUTANE problem was reported by a Physician from UNITED KINGDOM on Feb 19, 2008. Female patient was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . ROACCUTANE dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Valtrex Side Effects Report #5644483-8
Consumer or non-health professional from UNITED STATES reported VALTREX problem on Jan 18, 2007. Female patient was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, pruritus, . VALTREX dosage: 1MG PER DAY. During the same period patient was treated with LIPITOR. Patient recovered.
ILL-DEFINED DISORDER : Valtrex Side Effects Report #5644888-5
VALTREX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . VALTREX dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Valtrex Side Effects Report #5644912-X
Consumer or non-health professional from UNITED STATES reported VALTREX problem on Oct 15, 2007. Female patient was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . VALTREX dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Valtrex Side Effects Report #5645003-4
VALTREX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 31, 2007. Male patient was diagnosed with ill-defined disorder and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . VALTREX dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Stilnox Side Effects Report #5645562-1
Consumer or non-health professional from AUSTRALIA reported STILNOX problem on Feb 19, 2008. Female patient was treated with STILNOX. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . STILNOX dosage: unknown. Patient died.
ILL-DEFINED DISORDER : Tegretol Side Effects Report #5647407-2
TEGRETOL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 29, 2008. Male patient was diagnosed with convulsion and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . TEGRETOL dosage: unknown. Patient recovered.
ILL-DEFINED DISORDER : Lyrica Side Effects Report #5583384-0
Consumer or non-health professional from UNITED STATES reported LYRICA problem on Dec 28, 2007. Female patient, weighting 149.9 lb, was diagnosed with diabetic neuropathy, diabetes mellitus and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . LYRICA dosage: unknown. During the same period patient was treated with AVANDIA, GLIPIZIDE. Patient recovered.
ILL-DEFINED DISORDER : Midazolam Side Effects Report #5589187-5
MIDAZOLAM problem was reported by a Pharmacist from UNITED STATES on Jan 10, 2008. Female patient, weighting 1.68 lb, was diagnosed with sedation and was treated with MIDAZOLAM. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . MIDAZOLAM dosage: 0.07 MG ONCE IV BOLUS (1 DOSE). Patient recovered.
ILL-DEFINED DISORDER : Morphine Side Effects Report #5593110-7
Consumer or non-health professional from UNITED STATES reported MORPHINE SULPHATE problem on Jan 14, 2008. Male patient, 65 years of age, was diagnosed with pain and was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, . MORPHINE SULPHATE dosage: 190 MG AM DOSE. Patient recovered.