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

DRUG INEFFECTIVE ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
RASH ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
SHOULDER ARTHROPLASTY ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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