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

NAUSEA ( 9 FDA reports)
DYSPNOEA ( 7 FDA reports)
DIZZINESS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
PAIN ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
VOMITING ( 4 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)

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