Please choose an event type to view the corresponding MedsFacts report:

VOMITING ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
AGITATION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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